Human Brain Disorders: A Review

Falaq Naz1, Yasir Hasan Siddique1, *
1 Department of Zoology, Faculty of Life Sciences, Drosophila Transgenic Laboratory, Section of Genetics, Aligarh Muslim University, Aligarh-202002, Uttar Pradesh, India

© 2020 Naz and Siddique.

open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

* Address correspondence to this author at the Department of Zoology, Faculty of Life Sciences, Drosophila Transgenic Laboratory, Section of Genetics, Aligarh Muslim University, Aligarh-202002, Uttar Pradesh, India; Tel: 0571-2700920-3447; E-mail:



Due to the stressful life, brain disorders are considered as a significant global healthcare problem. It has generated a great need for continuous research for understanding brain structure as well as functions in context to health and diseases.

Scope and Approach:

The structure and functions of the brain were questioned and studied since Ancient Greek times and led to the compilation of enormous information on the subject globally. With the advent of new technology, the researchers are able to discover the causes of brain diseases/disorders.


In the present review, we have compiled various diseases and disorders related to the brain, along with their symptoms and the treatment strategies.

Keywords: Brain, Disorder, Human, Neuron, Diseases, Neurodegeneration.


The brain is the command center of the Central Nervous System (CNS) made up of a large mass of nerve cells, protected in the skull [1-3]. It has three main parts i.e. the cerebrum, the brainstem, and the cerebellum. It controls the intellectual activities of the body, like processing, integrating, and coordinating the information received from the sensory organs. It is a jelly-like mass of tissue, weighing about 1.4 kg, and containing 86 billion nerve cells [4-7]. The cerebrum is connected to the brainstem, which, on the other end, connects to the spinal cord. The brainstem consists of three parts, namely the midbrain, the pons, and the medulla oblongata. Underneath the cerebral cortex, there are several brain structures, namely the thalamus, the pineal gland, the hypothalamus, the pituitary gland, the amygdala and the hippocampus. The cross-section of each cerebral hemisphere shows a ventricle cavity where the cerebrospinal fluid is produced and circulated. Below the corpus callosum is the septum pellucidum, a membrane that separates the lateral ventricles [8, 9]. The cerebrum is the largest part of the human brain. It is divided into two cerebral hemispheres, having two-third of the total weight of the brain. One hemisphere is functionally dominant and controls language and speech. The other hemisphere interprets visual and spatial information. The two hemispheres of the human brain, the left and right, are connected together by a bundle of nerve fibers called the corpus callosum. Each hemisphere is divided into four lobes, namely the frontal lobe, temporal lobe, parietal lobe, and occipital lobe [10-13]. The frontal lobe controls cognitive functions and voluntary movements or activities such as emotional expression, problem-solving, memory, language, judgment, and sexual behaviors [14]. The temporal lobe controls the primary auditory perceptions such as hearing, and contains the primary auditory cortex, which receives the sensory information from the ears and secondary areas, and process information into meaningful terms which are expressed in the form of speech and words [15]. The parietal lobe processes information about temperature, taste, touch, and movement [14]. The occipital lobe is primarily responsible for vision [16].


The brain cells are referred as neurons and the supporting non-neuron cells are called glial cells. The average adult human brain contains approximately 86 billion neurons. It was suggested by many researchers that both neurons and glial cells are necessary for the proper functioning of the brain. Neurons in the brain are responsible for sending and receiving electrical and biochemical signals [17]. The neuron is made up of three basic parts: the cell body or soma, branching dendrites, and the axon. They are building blocks of the brain and transmit information to other neurons, muscles and tissues throughout the body.

Fig. (1). Major human neurodegenerative diseases and neuropsychiatry disorders.

Neurons help to think, feel, move, and comprehend the world around us. Glia cells are also very important cells of the nervous system. The name “glia” is the Latin word for “glue” [18]. The glial cells actively participate in brain signaling and are necessary for the healthy functioning of neurons. There are many types of glial cells in the brain. The three important types of glial cell are Oligodendrocytes: which help in insulating the axons and to pass the electrical signals properly at incredible speed over long distances; Microglia: also known as immune cells of the CNS, move around within the brain and constantly communicate with other glia cells; Astrocytes: These are star-shaped cells supporting to the Blood-Brain Barrier (BBB), provide nutrients to the neurons, repair the nervous tissue, and facilitate neurotransmission [19-21].


Blood vessels are critical in delivering oxygen and nutrients to all the tissues and organs throughout the body. The blood vessels system of CNS is unique, constituting the BBB, which allow these vessels to tightly regulate the movement of ions, molecules, and cells between the blood and the brain [22]. The purpose of the BBB is to protect it against circulating toxins or pathogens, while at the same time allowing the vital nutrients to reach the brain. BBB is formed by the brain capillary endothelium [23]. It also maintains the level of hormones, nutrients and water in the finely tuned brain environment [24]. The delivery of therapeutic agents to the specific regions of the brain is a major challenge in the treatment of almost all types of brain disorders. The BBB hampers the delivery of many potentially important diagnostic and therapeutic agents to the brain. Therapeutic molecules and antibodies that might otherwise be effective in therapy do not cross the BBB in sufficient amount [25].


Any deformities, dysfunction and disease condition in the brain affect the whole body. The brain is susceptible to neuronal disease and neurons or tissue infection. Damage can be caused by trauma (psychiatric condition), or a loss of blood supply (accidental or environmental factors) known as a stroke. In brain injury, the degeneration of brain cells occurs [26, 27]. It depends upon a wide range of internal as well as external factors. Brain damage due to trauma is induced by personal factors or mentally unstable conditions, while neurotoxicity refers to chemically induced neuronal damage [26]. Broadly human brain disorders are divided into two categories namely, Neurodegenerative diseases and Neuropsychiatric disorders (Fig. 1). Both are tough to understand and incurable, but there are medicines, surgery and physical therapies applied for the treatment or to suppress the symptoms of the diseases (Table 1) [28-124].

Table 1. Types of human brain diseases/disorders with their symptoms and treatments (Source:
Category S.No. Type of Diseases/
Parts of the Brain affected Symptom(s) Treatment(s) Reference(s)
Autoimmune Diseases 1. Autoimmune encephalitis Brain cells Impaired memory and cognition, abnormal movements, seizures, and problems with balance, speech, or vision, psychosis, aggression, inappropriate sexual behavior, panic attacks, compulsive behaviors and euphoria or fear. Intravenous immunosuppressive therapy and tumor removal. [28,29]
2. Autoimmune
Brain cells Recurrent and uncontrolled seizures. Corticosteroids in addition to intravenous immunoglobulin or plasma exchange. [30,31]
3. Central nervous system vasculitis Inflammation of blood vessels in the Brain Headaches, strokes or transient ischemic attacks,
forgetfulness or confusion
weakness, problems with eyesight, seizures and
encephalopathy (swelling of the brain).
High-dose steroids such as prednisone, in combination with cyclophosphamide. [32,33]
4. Hashimoto’s encephalopathy Lymphocytic vasculitis of venules and veins in the brain-stem and a diffuse gliosis involving gray matter or white matter Personality changes, aggression, delusional behavior, concentration and memory problems, coma, disorientation, headaches, jerks in the muscles, lack of coordination, partial paralysis on the right side, psychosis, seizures (60% cases), sleep abnormalities, speech problems and tremors. Corticosteroids [34,35]
5. Neuromyelitis optica Eye nerves and spinal cord (myelin) Blindness in one or both eyes, weakness or paralysis in the legs or arms, painful spasms, loss of sensation, uncontrollable vomiting and hiccups, and bladder or bowel dysfunction from spinal cord damage. Intravenous corticosteroids and low doses of carbamazepine. [36,37]
6. Optic neuritis Fatty coating (myelin) and optic nerve is inflamed. Vision gets dim or blurry and loss of colour vision. Intravenous immune globulin and vitamin B12. [38, 39]
7. Neurosarcoidosis or neurosarcoid Facial and cranial nerves, hypothalamus Bell’s palsy, leading to one-sided weakness of the facial muscles, double vision, hearing loss, headaches, speech problems, irritability, memory loss, changes in mood, dementia, hallucinations and seizures. Corticosteroids, immunosuppressive medication, pain medication, radiation therapy, occupational and physical therapy. [40, 41]
8. Neuro-Behcet’s disease Ventral brain stem Fever, headache, genital ulcers, genital scars and skin lesions. Azathioprine or methotrexate and corticosteroids. For high risk of patients intravenous cyclophosphamide with corticosteroids. [42,43]
9. Cerebral lupus or Systemic Lupus Erythematosus (SLE) Brain cells Fatigue, fever, joint pain, stiffness and swelling, butterfly-shaped rash on the face, skin lesions, fingers toes turn white or blue when exposed to cold or during stress, shortness of breath, chest pain and dry eyes. Nonsteroidal anti-inflammatory drugs (NSAIDs) such as naproxen sodium (Aleve) and ibuprofen, antimalarial drugs such as hydroxychloroquine (plaquenil), corticosteroids prednisone,
Immunosuppressants azathioprine (imuran, azasan), mycophenolate mofetil and methotrexate and rituxan.
10. Autism or Autism Spectrum Disorder (ASD) Hippocampus, amygdala, lobes of the cerebrum ventricles and caudate nucleus. Adoption of unusual speech patterns, such as using a robot-like tone, avoiding eye contact with others, not able to responding to their name, late development of speech skills, having difficulty with maintaining conversation, frequently repeating phrases, apparent difficulty in understanding feelings and expressing their own. Behavior and communication treatments like play therapy, behavioral therapies, sensory therapies, occupational therapy, speech therapy, and only one medicine i.e. risperidone (risperdal). [46, 47]
Dementia 1. Fronto-temporal dementia Degeneration of the temporal and frontal lobes. Poor judgment, loss of empathy, socially inappropriate behavior, lack of inhibition, repetitive compulsive behavior, inability to concentrate or plan; frequent abrupt mood changes, speech difficulties. Antidepressant drugs and Antipsychotic drugs. [48, 49]
2. Dementia with Lewy bodies Clumps of a protein in the cortex. Sleep disturbances, hallucination, imbalance, movement difficulties. Cholinesterase inhibitors, carbidopa and levodopa (sinemet, rytary, duopa). [50, 51]
3. Vascular dementia Blocking of blood vessels. Problems with short-term memory, laughing or crying at inappropriate times, trouble in concentrating, planning, or trouble in managing money, inability to follow instructions, loss of bladder or bowel control and hallucinations or delusions. High blood pressure under control through exercise, diet and medication. [52, 53]
4. Alzheimer’s Disease (AD) Destroy neurons and their connections in parts of the brain and affects areas in the cerebral cortex (plaque accumulation of abnormally folded amyloid β-protein and tau protein in the brain). Having less energy, less interest in work and social activities, loss of memory, like forgetting conversations and events that just happened, language problems, coordination problems, mood swings and depression. Donepezil (Aricept), Rivastigmine (Exelon), Tacrine (Cognex) [54, 55]
Brain Infections 1. Meningitis Inflammation of the meninges, brain and spinal cord. Decreased appetite, irritability, sleepiness, lethargicity, fever, sensitivity to bright light, sleepiness, nausea, vomiting, confusion and disorientation. Antibiotics given directly into a vein, fluids given directly into a vein to prevent dehydration, oxygen through a face mask if there are any breathing difficulties, steroid medication to reduce any swelling around the brain. [56, 57]
2. Encephalitis Temporal lobe, frontal lobe Headache, fever, aches in muscles or joints, fatigue or weakness, confusion, agitation or hallucinations, seizures, loss of sensation or paralysis in certain areas of the face or body, muscle weakness, problems with speech or hearing and loss of consciousness. Corticosteroids, acyclovir (Zovirax) and ganciclovir (Cytovene). [58, 59]
3. Brainabscess Fungal and viral infection in brain Differences in mental processes, such as increased confusion, decreased responsiveness, and irritability, speech, sensation, decreased movement due to the loss of muscle function, changes in vision, changes in personality or behavior, vomiting, fever, chills, neck stiffness, especially when it occurs with fever and chills, sensitivity to light. Antibiotic medications and surgery. [60, 61]
Movement Disorders 1. Ataxia Cerebellum Poor coordination, unsteady walk and a tendency to stumble, difficulty with fine motor tasks, such as eating, writing or buttoning a shirt, change in speech, involuntary back-and-forth eye movements (nystagmus) and difficulty in swallowing. Occupational therapy, speech and language therapy, physical and mental exercise. [62, 63]
2. Dystonia and Cervical dystonia Basal ganglia Dragging leg, cramping of the foot, involuntary pulling of the neck, uncontrollable blinking and speech difficulties. Levodopa, procyclidine, hydrochloride, diazepam, lorazepam, clonazepam and baclofen [64, 65]
3. Chorea Basal ganglia Problem in speaking, swallowing, posture and gait. Medication like Fluphenazine (Prolixin), Haloperidol (Haldol), Olanzapine (Zyprexa), Quetiapine (Seroquel), Risperidone (Risperdal). [66, 67]
4. Huntington’s Disease (HD) Nerve cells and basal ganglia Involuntary jerking or writhing movements, muscle problems, such as rigidity or muscle contracture, slow or abnormal eye movements, impaired gait, posture and balance, difficulty in speech or swallowing. Medication like Tetrabenazine (Xenazine), antipsychotic drugs, such as Haloperidol (Haldol) and Chlorpromazinamantadine, Levetiracetam (Keppra, others) and Clonazepam (Klonopin). [68, 69]
5. Multiple System Atrophy (MSA) Cerebellum, basal ganglia and brainstem Impaired movement and coordination, such as unsteady gait and loss of balance, slurred, visual disturbances, difficulty swallowing (dysphagia) or chewing, constipation, agitated sleep due to “acting out” dreams, abnormal breathing at night, inability to achieve or maintain an erection, loss of libido, irregular heartbeat and difficulty in controlling emotions. Corticosteroid Fludrocortisone, Epyridostigmine (Mestinon), Midodrine Levodopa and Carbidopa (Duopa, Sinemet). [70, 71].
6. Myoclonus Cerebral cortex, cerebellum and brainstem Sudden, brief, involuntary, shock, variable in intensity and frequency, localized to one part of the body or all over the body, sometimes severe enough to interfere with eating, speaking or walking. Tranquilizers like Clonazepam (Klonopin), anticonvulsants like Levetiracetam (Keppra, Roweepra, Spritam), Valproic acid (Depakene) and Primidone (Mysoline), Piracetam
onabotulinumtoxin A (Botox) injections, deep brain stimulation (DBS).
7. Parkinson’s Disease (PD) Nerve cells, basal ganglia and substantia nigra Tremor, shaking hand or fingers, slowed movement (bradykinesia), rigid muscles, impaired posture and balance, loss of automatic movements, speech changes and writing changes. Levodopa, the most effective
carbidopa-levodopa infusion, dopamine agonists, MAO-B inhibitor, catechol O-methyltransferase (COMT) inhibitors, anticholinergics, amantadine, DBS.
[74, 75]
8. Progressive supra-nuclear palsy or Steele-Richardson-
Olszewski syndrome
Basal ganglia and the brain stem Stiffness and awkward movements, problems with speech and swallowing, sensitivity to light, sleep disturbances, loss of interest in pleasurable activities, impulsive behavior, possibly including laughing or crying for no reason, difficulties with memory, reasoning, problem-solving and decision-making, depression and anxiety. Physical and occupational therapy, medication like onabotulinum toxin type A (Botox), eyeglasses with bifocal or prism lenses. [76, 77]
9. Restless Legs Syndrome (RLS) Cingulate cortex and cerebellum Sensations after rest, worsening of symptoms in the evening and night, time leg twitching. Ropinirole (Requip), Rotigotine (Neupro), Pramipexole (Mirapex), Gabapentin (Neurontin, Gralise), Gabapentin Enacarbil (Horizant), Pregabalin (Lyrica), Tramadol (Ultram, ConZip), Codeine, Oxycodone (Oxycontin, Roxicodone, others) and Hydrocodone (Hysingla ER, Zohydro ER), muscle relaxants and sleep medications. [78, 79]
10. Tardive dyskinesia Striatum and basal ganglia Tongue movements, lip smacking, lip puckering, pursing of the lips and excessive eye blinking Medication like Deutetrabenazine (Austedo)
Valbenazine (Ingrezza), Melatonin, Vitamin B6, Vitamin-E
11. Tourette syndrome Basal ganglia Eye blinking, head jerking, repeating observed movements, shoulder shrugging, stepping in a certain pattern, eye darting, obscene gesturing, nose twitching, bending or twisting, mouth movements and hopping. Medications that block or lessen dopamine, botulinum (Botox) injections, ADHD medications, central adrenergic inhibitors anti-depressants, anti-seizure medications, behaviour therapy, psychotherapy and deep brain stimulation. [82, 83]
12. Wilson's disease Brain and spinal cord Fatigue, lack of appetite or abdominal pain, yellowing of the skin and the white of the eyes (jaundice), golden-brown eye discoloration (Kayser-Fleischer rings), fluid buildup in the legs or abdomen, problems with speech, swallowing or physical coordination and uncontrolled movements or muscle stiffness. Medication like Penicillamine (Cuprimine, Depen), Trientine (Syprine), T-Zinc acetate (Galzin) and Surgery. [84, 85]
Neuromuscular Diseases 1. Amyotrophic Lateral Sclerosis (ALS) Degeneration of nerve cells in the spinal cord and brain. Twitching and cramping of muscles, loss of motor control in the hands and arms, impairment in the use of the arms and legs, tripping and falling, dropping things, persistent fatigue, uncontrollable periods of laughing or crying, slurred or thick speech and trouble in projecting the voice. Physical, occupational, speech, respiratory, and nutritional therapies. [86, 87]
2. Charcot-Marie-Tooth disease Axon (myelin sheath) Weakness of foot and lower leg muscles, foot deformities,
difficulty in lifting foot while walking, loss of muscles around hands and feet, numbness, tingling, burning, or loss of temperature sensation in hands and feet, discomfort or pain in hands and feet.
Physical therapy, occupational therapy, orthopedic devices, pain relieving medicines. [88, 89]
3. Multiple sclerosis Brain, spinal cord and nerve cells Blurred or double vision, red-green color distortion, pain and loss of vision because of swelling of the optic nerve (optic neuritis), trouble in walking, numbness, prickling, or pins and needles (paresthesia), muscle weakness in the arms and legs, trouble with coordination, fatigue, loss of feeling, speech problems, tremors, dizziness, hearing loss, bowel and bladder problems and depression. Exercise programs that build muscle strength, endurance, and control. [90, 91]
4. Muscular dystrophy Absence of protein dystrophin in neurons Progressive muscle weakness and wasting (atrophy), waddling way of walking, difficulty in climbing stairs, repeated falling, curvature of the spine, wasting of thigh muscles, abnormal enlargement of the calves, trouble in breathing and swallowing and enlargement of the heart. Physical therapy and exercise, Surgery and Prednisone. [92, 93]
5. Myasthenia gravis Neurons Visual problems including drooping eyelids (ptosis) and double vision (diplopia), muscle weakness and fatigue, weakness of the neck or limbs. Anti-cholinesterase medicines, steroids, or medicines that suppress the immune system’s response, thymectomy and plasmapheresis [94, 95]
6. Myositis, including polymyositis and dermatomyositis Bubbles in the brain Muscle weakness, painful muscles, extreme tiredness, generally feeling unwell, shortness of breath. Exercise and physiotherapy, steroid medication, Intravenous immunoglobulin therapy, Rituximab injection [96, 97]
7. Peripheral neuropathy Nerves in the brain and brainstem Gradual onset of numbness, jabbing, throbbing or burning pain, lack of coordination, muscle weakness, paralysis if motor nerves are affected. Pain relievers, anti-seizure medications, topical treatments, antidepressants, therapies, transcutaneous electrical nerve stimulation (TENS). [98, 99]
8. Spinal muscular atrophy Spinal cord and brain stem Muscle weakness and twitching, difficulty in breathing and swallowing, changes in the shape of the limbs, spine, and chest due to muscle weakness, difficulty in standing and walking. Drugs such as spinraza and zolgensma. [100, 101]
Seizure Disorders 1. Tonic-clonic seizures or Grand- mal seizure Cerebellum, basal ganglia, brainstem and thalamus. Loss of bowel and bladder control, unresponsiveness after convulsions, confusion, fatigue and severe headache. Drugs like carbamazepine (Carbatrol, Tegretol), Phenytoin (Dilantin, Phenytek), valproic acid (Depakene), oxcarbazepine (Oxtellar, Trileptal), Lamotrigine (Lamictal), Gabapentin (Gralise, Neurontin), Topiramate (Topamax), Phenobarbital and Zonisamide (Zonegran) [102, 103]
2. Atonic seizures Alterations in brain function A sudden loss of muscle strength, going limp and falling to the ground, if seated, the person’s head will appear to suddenly drop down, remaining conscious, drooping eyelids, head nods and jerking movements. Ethosuximide (Zarontin) and Valproic acid (Depakene) [104, 105]
3. Myoclonic seizures Temporal lobe Sudden increases in muscle tone, sudden spasm, occasionally and falling asleep. Anti-seizure medication, nerve stimulation, dietary therapy or surgery. [106]
4. Absence seizures or Petit mal seizures Thalamus Sudden stop in motion without falling, lip smacking, eyelid flutters, chewing motions, finger rubbing and small movements of both hands. Ethosuximide (Zarontin), Valproic acid (Depakene) and Lamotrigine (Lamictal). [107,108]
Stroke Diseases 1. Trauma Alterations in brain functioning. Loss of consciousness for a few seconds to minutes, confused or disoriented state of mind, headache, nausea or vomiting, fatigue or drowsiness, problems with speech, difficulty in sleeping, dizziness and loss of balance. Immediate emergency care, medication, surgery and rehabilitation. [109, 110]
2. Tumors Brain cells Headache, nausea, vomiting, vision problems: such as blurred vision, double vision or loss of peripheral vision, gradual loss of sensation or movement in an arm or a leg, speech difficulties and hearing problems. Medication, surgery, rehabilitation, minimally invasive scar less brain surgery, radiation therapy, chemotherapy and targeted drug therapy. [111, 112]
Mental Disorders 1. Anxiety disorders, including panic disorder, obsessive-compulsive disorder, and phobias Amygdala Fatigue, trouble in sleeping, muscle tension or muscle ache, trembling, feeling twitchy, nervousness, sweating, nausea, diarrhea and irritability. Psychotherapy, drugs like antidepressants, buspirone, benzodiazepines are used. [113, 114]
2. Post-traumatic stress disorder Cingulate cortex and frontal gyrus Negative thoughts, memory problems, difficulty in maintaining close relationships and emotionally numb. Psychotherapy, cognitive therapy, eye movement desensitization and reprocessing (EMDR).
Medications like anti-depressants and anti-anxiety (Prazosin).
3. Psychotic disorders, including schizophrenia Medial frontal lobe Delusions, hallucinations, disorganized thinking (speech), extremely disorganized or abnormal motor behavior, negative symptoms, sleep disturbances, irritability or depressed mood and lack of motivation. Cornerstone, antipsychotic medications, aripiprazole (abilify), asenapine (saphris), brexpiprazole (rexulti), paliperidone (invega), quetiapine (seroquel), risperidone (risperdal), ziprasidone (geodon) and long-acting injectable antipsychotics. [117, 118]
4. Depression, bipolar disorder, and other mood disorders Hippocampus Increased activity, energy or agitation, exaggerated sense of well-being and self-confidence (euphoria), sleep disturbances, unusual talkativeness or making foolish investments. Mood stabilizers, anti-psychotics, anti-depressants, antipsychotic and anti-anxiety medications. [119, 120]
5. Eating disorders Brain cells Abnormally low body weight, intense fear of gaining weight, repeatedly and persistently regurgitating food after eating. Healthy eating, psychotherapy, family-based therapy (FBT), cognitive behavioral therapy (CBT), antidepressants and anti-anxiety medications. [121, 122]
6. Personality disorders Amygdala, pre-frontal cortex Aggression toward people and animals, destruction of property deceitfulness, theft, serious violation of rules, exploit others, poor or abusive relationships, being consistently irresponsible. Psychotherapy [123, 124]

4.1. Neurodegenerative Diseases

Neurodegenerative Diseases are a composite form of disorders characterized by progressive loss of neurons, which hamper the function of the Central Nervous System (CNS) as well as Peripheral Nervous System (PNS). These diseases show their impact on both mental as well as and physical activity of the human body such as, movement, speech, memory, intelligence and coordination. The causes of these diseases are not specific due to the similarity in symptoms. Some common neurodegenerative diseases are Alzheimer’s Disease (AD), Parkinson’s Disease (PD), Prion disease, Huntington’s Disease (HD), Spino-Cerebellar Ataxia (SCA) and Spinal Muscular Atrophy (SMA) [125]. In AD, neuron death has been reported amygdala, cortex, and hippocampal region of the brain [126]; while in PD, substantia nigra pars compacta shows neuronal death that leads to the deficiency of dopamine [127].

Alzheimer’s Disease (AD) is the most prevalent and mainly affects the population of above 60 years. It was first described in 1906 by German Physician Alois Alzheimer on the basis of a medical case of Auguste D, a patient who showed symptoms of memory loss and some psychological changes like mood swing and unresponsive behavior. AD was named after German Doctor Alois Alzheimer by Emil Kraepelin, who was the colleague of Dr. Alzheimer. In 1910, he mentioned for the first time this disease as “Alzheimer’s disease” in his medical book named ‘Psychiatrie’ [128, 129]. It is charac- terized by progressive memory loss and cognitive impairments. Mainly two proteins are responsible for causing this disease i.e., beta-amyloid (β) and tau protein which show a high amount of accumulation in the brain. Both proteins may lead to the degeneration of neurons [126]. The pathological hallmark of AD includes, the presence of extracellular amyloid β plaques and formation of intracellular neurofibrillary tangles that leads to synaptic dysfunction, neuronal loss, and brain atrophy [130].

Parkinson’s Disease (PD) is the second most common neurodegenerative disease after AD. It is a progressive CNS disorder that affects mainly the movement of the body. It affects both motor as well as non-motor functions. The causes of PD are still unknown, but the involvement of both genetic and environmental factors considered to be responsible for the progression of the disease. It was described by Dr. James Parkinson (1817) in his monograph entitled “An Essay on the Shaking Palsy” [131, 132]. It is characterized by the loss of dopaminergic neurons and the accumulation of Lewy bodies in the substantia nigra pars compacta of the mid brain. Clinical symptoms mainly involves rigidity, akinesia, tremors, postural instability, and non-motor symptoms [133].

In 1920, Neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob describe prion disease as a human neurological disorder. Prion disease is also known as Transmissible Spongiform Encephalopathies (TSEs) and is characterized as rare progressive neurodegenerative disorders which not only affect humans but also animals [134]. In this disease a normal cell surface glycoprotein (PrPC) is converted into conformational altered isoform i.e. (PrPSc) . PrPSC is responsible for the neurological disorder [135]. The most common form of prion disease that affects human is Creutzfeldt-Jakob Disease (CJD) and animal (cows) bovine spongiform encephalopathy (BSE or ‘mad cow’ disease). Prions are protein that are misfolded and also have the property to propagate [136, 137].

Huntington’s Disease (HD) is also known as Huntington’s chorea. It results due to the progressive degeneration of neuronal cells in the brain. George Huntington, described it in 1872 as a hereditary neurodegenerative disease [138]. It is an autosomal-dominant neurodegenerative disease which results from the unstable trinucleotide repetition of Cytosine-Adenine-Guanine (CAG). It is clinically characterized by involuntary movements, cognitive decline, and behavioral changes [139].

4.2. Neuropsychiatry Disorders/Conditions

Neuropsychiatry is a kind of disorder or conditions that deals with mental disruption which results due to the improper functioning of the brain. It is defined as mental disorders or disorders of the brain [140]. According to Berrios and Markova,, neuropsychiatry explains about brain having some lesions that disfigured the brain leading to mental disorder [141]. Neuropsychiatric disorders severely affect the well-being of a person with a negative impact on general health. It hampers the ability of learning (childhood) and inability of focusing or concentrating in work (adulthood) [141, 142]. They are complex and hard to understand because of the similarity in symptoms. Some common neuropsychiatric disorders are seizures, attention or cognitive deficit disorders, uncontrollable anger, migraine headaches, addictions, eating disorders, depression and anxiety. The person suffering from neuropsychiatry disorders shows changes in behavior i.e. aggression, violence, criminal activity, antisocial personality disorder, psychopathy, impulse control disorders and episodic dyscontrol [143, 144]. The causes of brain disorders are still unclear, but some genetic as well as environmental factors are responsible for the diseased condition. These disorders have a relatively high prevalence and show early onset (autism in childhood and schizophrenia in adulthood) [145, 146]. Table 1 summarizes the different categories of brain disorders with their symptoms and preventions.


The role of genes and the environment for the progression of neurological disease/disorders cannot be ignored. Any damage to the CNS leads to cell death which leads to the loss of function [147]. The brain disorders hampered the normal functioning of the brain and lead to the progressive decline or sudden complete loss of brain functions (sensory, motor, and cognitive) [148]. There are some neurodegenerative diseases which are characterized by the abnormal accumulation of the protein in the brain tissue i.e. Tau protein, β-amyloid (accumulation of plaques in the form of neurofibrillary tangles) in AD, misfolded Huntingtin protein in HD, aggregation of ubiquitinated proteins in ALS, α-synuclein accumulation in PD, and cell surface glycoprotein accumulation in prion disease [149-152]. Some studies have suggested that the mutation in genes leads to the accumulation of misfolded protein. Physical injury to the brain may lead to synaptic insufficiency, massive cell death and inflammation that may lead to temporary or permanent loss of various bodily actions like coordination in the movement (ataxias) and different cognitive functions like memory, learning, decision-making skills, talking and dementia. There is no permanent treatment for neurodegenerative diseases. In advanced stages of the diseases, DBS and cell transplantation therapies are used for controlling/reducing the physiological as well as cognitive deficits [153-155].

In AD, aggregation of β-amyloid protein accelerates the formation of neurofibrillary tangles which leads to synaptopathy in the form of glial inflammation and neuronal cell death in the cerebral cortex, sub-cortical regions, temporal lobes, parietal lobes, and cingulate gyrus in brain [156]. In PD the depletion of dopamine producing neurons in substantia nigra is accelerated by the intracellular accumulation of protein α-synuclein bound to ubiquitin complex. These protein aggregates form cytoplasmic inclusions in the form of Lewy bodies, which play a significant role in familial as well as sporadic cases of PD [133]. Similarly, HD is also caused by the intracellular accumulation of Huntingtin protein. The mutation in huntingtin (gene) results in the death of cells in the striatum region of the brain [138]. Multiple Sclerosis (MS) is a glial disorder. It involves massive damage to myelinated fibers through autoimmune reaction, causing axonal injury and further loss of neuronal communication mostly in the white matter tracts, the basal ganglia, and the brain stem [157]. It has been reported that the genetic factors responsible for AD ranges from 49-79% [156]. Similarly, for PD it ranges from 5-10% [156]. While, HD is considered as a pure genetic disorder which is caused by tri-nucleotide repeat expansions (CAG) nucleotides [138]. The whole genome sequence may help both researchers as well as clinicians to understand the genetic factors that play an important role in health, disease, and drug response [158]. The interplay of genetic and environmental factors that hampers the brain function is difficult to understand [159]. It was studied that in schizophrenia and bipolar disorders, genetic factors play a huge role in the development of disease. In a twin study, it ranges from 70-80%. Similarly, in depression, the genetic factors showed significant increment of 38% to 75% [160, 161]. In dementia cases, 1 in 4 person aged above 55 has a family history of dementia [162].

Dementia is an umbrella term used to demonstrate a group of symptoms in neurodegenerative diseases. The late stages of the neurodegenerative diseases lead to significant cognitive dysfunctions that are enough to affect a routine life. The symptoms of Dementia shows deficits in memory and learning, impairment in visual, loss of attentive function, as well as behavioral disturbances [162]. Epigenetic factors also play an important role in aggravating the symptoms or enhancing the disease like symptoms. Some metals have been reported to contribute for the progression of AD and PD i.e. lead (Pb), Mercury (Hg), Arsenic (As), Cadmium (Cd), Almuniun [163, 164]. Pesticides also play an important role in neurological disorders like Paraquat (PQ) and 1-methy l-4 phenyl l-1, 2, 3, 6-tetrahydropyridine (MPTP) [165]. Rotenone, like Trichloroethylene (TCE) and toxic nanoparticles have also been shown to cause neuronal cell damage and improper functioning of the CNS [166, 167].


Due to the complex pathophysiology and overlapping of symptoms in various neurodegenerative diseases it is the need of the hour to build a database for neurodegenerative diseases. Researchers have developed an online web database (DND: Database of neurodegenerative disorders) that contains more than 100 neuro related disease concepts having the information of all related genes, their products, pathophysiological pathways and treatment strategies [168]. It provides enormous data related to almost every aspect of neurodegenerative disorders for better understanding of molecular and genetic pathways involved in the progression as well as treatment of the disease [168]. Researchers from University of Pennsyl- vania, with the help of a consortium of Penn investigators, have developed a novel Integrated Neurodegenerative Disease Database (INDD) for AD, PD, ALS and Fronto-temporal lobar degeneration [169]. This database (Penn INDD) has the ability to query multiple database tables from a single console with a high degree of precision and reliability. It is also useful for comparative studies of various neurodegenerative diseases [169]. Kandale et al. [170] have included 18 diseases in Integrated Database of Neurodegenerative Diseases (IDND). They have prepared IDND by using three separate databases i.e. UniProt kB (protein information), kEGG (Pathway), PubMed (disease articles).

PD Gene is another dedicated online resource that comprehensively collects and meta-analyzes all published studies in the related field [171]. This database help researchers to decipher the genetic architecture underlying PD susce- ptibility. With the help of this database ITGA8 was identified as a novel potential PD risk locus [171].

Alz Data is related to the most prevalent and rapidly increasing neurodegenerative disorder i.e., Alzheimer’s disease. This database includes: (i) High throughput omic data e.g. Genomics (GWAS and Whole Exome Sequencing), Transcriptomes, Proteomics and Functional genomics; (ii) High Confident functional data, e.g. neuroimaging screening, population base longitudinal studies and transgenic mouse phenotyping [172].

Schizophrenia is one of the common psychiatric disorders having heritability of about 80% [173]. The genetic and molecular studies carried out on Schizophrenia have been deposited in database i.e. SZDB. Recently, a new version of a comprehensive database for Schizophrenic research has been launched i.e. SZDB 2.0 ( [174]. The new version includes Genomes Wide Association Study (GWAS), polygenic risk score calculator, genetic and gene expression studies, copy number variations, gene expression Quantitative Trait Loci (eQTL), transcript QTL, methylation QTL and protein-protein interaction data [174]. This database will definetly provide a good platform for the enhancement of the Schizophrenia research.

BD gene is another database that was designed to address the genetic complexities of Bipolar Disorder (BD) and its overlapping with Schizophrenia as well as Major Depressive Disorder (MDD) [173]. It is freely available for the researchers. It provides not only a detailed review of research but also provides details for high confidence candidate genes and pathways for better understanding the pathology of the disease [173].


A number of animal model such as Caenorhabditis elegans, Drosophila melanogaster (fruitfly), Musca domestica (house fly), Danio rerio (zebra fish), pig and monkeys are used for understanding molecular pathways involved in various categories of brain disorders/diseases [175]. Cell lines are also used to explore the molecular pathways involved in the progression of brain diseases/disorders. Recent studies have revealed a great similarity between monkey and human brain (both in structure as well as in organization). It is expected that it will help a lot in understanding human brain diseases/disorders [176]. However, the selection of the model depends on the nature of the biological questions to be answered [176]. C. elegans has been used as a model organism for studying various aspects of neurodegenerative diseases like PD [177], AD [178], and HD [179], due to the conserved counterparts in C. elegans. The improved transgenic technology has led Drosophila as a model for number of neurodegenerative disorders such as AD, taupathies, PD, amyotrophic sclerosis, hereditary spastic paraplegia and various polyglutamine diseases [180-182]. Zebra fish genes and their human homologues have conserved functions with respect to the etiology of neurodegenerative diseases including PD, HD and AD [183]. The larvae of Zebrafish display neuro-pathological and behavioral phenotypes that are quantifiable and comparable to humans [184]. By using genetic manipulation techniques, transgenic mice and rats have been developed to understand the pathophysiology of autism, Fragile X syndrome (FXS) and other neuropsychiatric disorders [185-187]. The cerebral cortex of pig, unlike that of mice or rat, has cerebral convolution (gyri and sulci) similar to human neo-cortex and thus is expected to yield high translational value [188]. The use of pig in neuroscience for the modeling of human brain disorders has been extensively reviewed by Lind et al. [189]. Pigs are more similar to humans than mice in anatomy, physiology and genome, hence genetically modified pigs are also being used to study various neurological disorders [190]. Neurological disorders have also been studied in transgenic monkeys [191]. Due to the highest similarity with humans, monkeys are preferred for understanding the pathways involved in the progression of PD [191], microcephaly [192], AD [193], and sleep disorders [194].

The brain neurons lack the potential of regeneration; hence, the aging degeneration leads to severe consequences of brain dysfunctions. The neurodegenerative diseases/disorders are characterized by slow progression at an early stage. These diseases affect elderly persons especially in developed countries where the life expectancy is high [195]. These diseases include Parkinson’s Disease (PD), Progressive Supra-nuclear Palsy (PSP), Multi-System Atrophy (MSA), Alzheimer's Disease (AD), Fronto-Temporal Dementia (FTD), and Dementia with Lewy Bodies (DLB). PD is a progressive neurodegenerative disorder that causes slowness of movement and rigidity in the body. It is characterized by neuronal loss in the substantia nigra and the other brain regions. It is associated with the formation of intracellular protein inclusions known as Lewy bodies (LBs) in the neurons [196, 197].

Nanotechnology has provided a platform for the transfer of drugs across the BBB. Researchers are trying to build liposomes, loaded with nanoparticles to gain access through the BBB [198, 199]. More research is required to determine effective strategies for the improvement of patients with brain disorders. Delivering drugs across the BBB is one of the most promising application of nanotechnology in the field of clinical neuroscience. Nanoparticles may potentially carry out multiple tasks in a pre-defined sequence, which may be important for the delivery of drugs across the BBB [200-204].


Due to the involvement of non-genetic factors in the progression of human brain disorders, the research has been focused more on the study of epigenetic factors. In this context the data available from the GWAS and the databases developed for neurodegenerative diseases have proven a great boon in the area. Although there are several models to study the neurodegenerative disease but still there is a need for other specialized techniques, especially for neuropsychiatric disorders due to the overlapping of symptoms. BD gene has attempted not only to address the genetic complexities of bipolar disorders but also overlapping symptoms of both schizophrenia and Major Depressive Disorders (MDD).


Not applicable.




The authors declare no conflict of interest, financial or otherwise.


Declared none.


[1] Nieuwenhuys R, Ten Donkelaar HJ, Nicholson C. The meaning of it all.The central nervous system of vertebrates 1998; 2135-95.
[2] Safi K, Seid MA, Dechmann DK. Bigger is not always better: when brains get smaller. Biol Lett 2005; 1(3): 283-6.
[3] Yuste R, Church GM. The new century of the brain. Sci Am 2014; 310(3): 38-45.
[4] Roth G, Dicke U. Evolution of the brain and intelligence. Trends Cogn Sci (Regul Ed) 2005; 9(5): 250-7.
[5] Jones EG, Mendell LM. Assessing the decade of the brain. Science 1999; 284(5415): 739.
[6] Striedter GF. Précis of principles of brain evolution. Behav Brain Sci 2006; 29(1): 1-12.
[7] Dhanwate AD. Brainstem death: A comprehensive review in Indian perspective. Indian J Crit Care Med peer-reviewed, official publication of Indian Society of Critical Care Medicine 2014; 18(9): 596.
[8] Butler AB. Chordate evolution and the origin of craniates: an old brain in a new head. Anat Rec 2000; 261(3): 111-25.
[9] Jarvis ED, Güntürkün O, Bruce L, et al. Avian Brain Nomenclature Consortium. Avian brains and a new understanding of vertebrate brain evolution. Nat Rev Neurosci 2005; 6(2): 151-9.
[10] Chiel HJ, Beer RD. The brain has a body: Adaptive behavior emerges from interactions of nervous system, body and environment. Trends Neurosci 1997; 20(12): 553-7.
[11] Glees P. The human brain 2005.
[12] Cosgrove KP, Mazure CM, Staley JK. Evolving knowledge of sex differences in brain structure, function, and chemistry. Biol Psychiatry 2007; 62(8): 847-55.
[13] Frigeri T, Paglioli E, de Oliveira E, Rhoton AL Jr. Microsurgical anatomy of the central lobe. J Neurosurg 2015; 122(3): 483-98.
[14] Müller WE, Eckert GP, Scheuer K, Cairns NJ, Maras A, Gattaz WF. Effects of β-amyloid peptides on the fluidity of membranes from frontal and parietal lobes of human brain. High potencies of A β 1-42 and A β 1-43. Amyloid 1998; 5(1): 10-5.
[15] Cowell PE, Turetsky BI, Gur RC, Grossman RI, Shtasel DL, Gur RE. Sex differences in aging of the human frontal and temporal lobes. J Neurosci 1994; 14(8): 4748-55.
[16] Frackowiak RS. Human brain function 2004.
[17] Aitken JT, Bridger JE. Neuron size and neuron population density in the lumbosacral region of the cat’s spinal cord. J Anat 1961; 95(1): 38-53.
[18] Jäkel S, Dimou L. Glial cells and their function in the adult brain: A journey through the history of their ablation. Front Cell Neurosci 2017; 11: 24.
[19] Yajima K, Suzuki K. Demyelination and remyelination in the rat central nervous system following ethidium bromide injection. Lab Invest 1979; 41(5): 385-92.
[20] Amat JA, Ishiguro H, Nakamura K, Norton WT. Phenotypic diversity and kinetics of proliferating microglia and astrocytes following cortical stab wounds. Glia 1996; 16(4): 368-82.
[21] Zheng D, Purves D. Effects of increased neural activity on brain growth. Proc Natl Acad Sci USA 1995; 92(6): 1802-6.
[22] Daneman R, Zhou L, Kebede AA, Barres BA. Pericytes are required for blood-brain barrier integrity during embryogenesis. Nature 2010; 468(7323): 562-6.
[23] Daneman R, Prat A. The blood-brain barrier. Cold Spring Harb Perspect Biol 2015; 7(1)a020412
[24] Tsuji A. Small molecular drug transfer across the blood-brain barrier via carrier-mediated transport systems. NeuroRx 2005; 2(1): 54-62.
[25] Ballabh P, Braun A, Nedergaard M. The blood-brain barrier: An overview: Structure, regulation, and clinical implications. Neurobiol Dis 2004; 16(1): 1-13.
[26] Clarke PGH, Oppenheim RW. Neuron death in vertebrate development: in vitro methods. Methods Cell Biol 1995; 46: 277-321.
[27] Finch CE, Day JR. Molecular biology of aging in the nervous system: a synopsis of the levels of mechanisms. Neurodegener Dis 1994; 33-50.
[28] Lancaster E. The diagnosis and treatment of autoimmune encephalitis. J Clin Neurol 2016; 12(1): 1-13.
[29] Venkatesan A. Epidemiology and outcomes of acute encephalitis. Curr Opin Neurol 2015; 28(3): 277-82.
[30] Levite M. Autoimmune epilepsy. Nat Immunol 2002; 3(6): 500-0.
[31] Britton J. Autoimmune epilepsy. Handb Clin Neurol 2016; 133: 219-45.
[32] Byram K, Hajj-Ali RA, Calabrese L. CNS vasculitis: An approach to differential diagnosis and management. Curr Rheumatol Rep 2018; 20(7): 37.
[33] John S, Hajj-Ali RA. CNS vasculitis. Semin Neurol 2014; 34(4): 405-12.
[34] Mocellin R, Walterfang M, Velakoulis D. Hashimoto’s encephalopathy: Epidemiology, pathogenesis and management. CNS Drugs 2007; 21(10): 799-811.
[35] Pinedo-Torres I, Paz-Ibarra JL. Current knowledge on Hashimoto’s encephalopathy: A literature review. Medwave 2018; 18(6): e7298.
[36] Weinshenker BG, Wingerchuk DM. Neuromyelitis spectrum disorders. Mayo Clin Proc 2017; 92(4): 663-79.
[37] Huda S, Whittam D, Bhojak M, Chamberlain J, Noonan C, Jacob A. Neuromyelitis optica spectrum disorders. Clin Med (Lond) 2019; 19(2): 169-76.
[38] Wilhelm H, Schabet M. The diagnosis and treatment of optic neuritis. Dtsch Arztebl Int 2015; 112(37): 616-25.
[39] Jenkins TM, Toosy AT. Optic neuritis: The eye as a window to the brain. Curr Opin Neurol 2017; 30(1): 61-6.
[40] Burns TM. Neurosarcoidosis. Arch Neurol 2003; 60(8): 1166-8.
[41] Bargagli E, Prasse A. Sarcoidosis: A review for the internist. Intern Emerg Med 2018; 13(3): 325-31.
[42] Ferreira BFA, Rodriguez EEC, Prado LLD, Gonçalves CR, Hirata CE, Yamamoto JH. Frosted branch angiitis and cerebral venous sinus thrombosis as an initial onset of neuro-Behçet’s disease: A case report and review of the literature. J Med Case Reports 2017; 11(1): 104.
[43] Kalra S, Silman A, Akman-Demir G, et al. Diagnosis and management of Neuro-Behçet’s disease: International consensus recommendations. J Neurol 2014; 261(9): 1662-76.
[44] Rahman A, Isenberg DA. Systemic lupus erythematosus. N Engl J Med 2008; 358(9): 929-39.
[45] Bărbulescu AL, Sandu RE, Vreju AF, et al. Neuroinflammation in systemic lupus erythematosus - A review. Rom J Morphol Embryol 2019; 60(3): 781-6.
[46] Miller-Kuhaneck H, Watling R. Autism: A comprehensive occupational therapy approach 2010.
[47] Patel VB, Preedy VR, Martin CR, Eds. Comprehensive guide to autism 2014.
[48] Finger EC. Frontotemporal Dementias Continuum (Minneap Minn) 2016; 22(2 Dementia): 464-89.
[49] Convery R, Mead S, Rohrer JD. Review: Clinical, genetic and neuroimaging features of frontotemporal dementia. Neuropathol Appl Neurobiol 2019; 45(1): 6-18.
[50] Cummings JL. The Neuropsychiatric Inventory: Assessing psychopathology in dementia patients. Neurology 1997; 48(5)(Suppl. 6): S10-6.
[51] Gomperts SN. Lewy body dementias: Dementia with Lewy bodies and Parkinson disease dementia. Continuum (Minneap Minn) 2016; 22(2 Dementia): 435-63.
[52] Hachinski V. Vascular dementia: A radical redefinition. Dementia 1994; 5(3-4): 130-2.
[53] Brust JC. Vascular dementia is overdiagnosed. Arch Neurol 1988; 45(7): 799-801.
[54] Mantzavinos V, Alexiou A. Biomarkers for Alzheimer’s Disease Diagnosis. Curr Alzheimer Res 2017; 14(11): 1149-54.
[55] Ballard C, Gauthier S, Corbett A, Brayne C, Aarsland D, Jones E. Alzheimer’s disease. Lancet 2011; 377(9770): 1019-31.
[56] Sakushima K, Hayashino Y, Kawaguchi T, Jackson JL, Fukuhara S. Diagnostic accuracy of cerebrospinal fluid lactate for differentiating bacterial meningitis from aseptic meningitis: A meta-analysis. J Infect 2011; 62(4): 255-62.
[57] Spach DH, Jackson LA. Bacterial meningitis. Neurol Clin 1999; 17(4): 711-35.
[58] Ellul M, Solomon T. Acute encephalitis - diagnosis and management. Clin Med (Lond) 2018; 18(2): 155-9.
[59] Roos KL, Tyler KL. Meningitis, Encephalitis, Brain Abscess, and Empyema Harrison’s Principles of Internal Medicine 19th ed. 2015.
[60] Brook I. Microbiology and treatment of brain abscess. J Clin Neurosci 2017; 38: 8-12.
[61] Brouwer MC, Coutinho JM, van de Beek D. Clinical characteristics and outcome of brain abscess: Systematic review and meta-analysis. Neurology 2014; 82(9): 806-13.
[62] Jones TM, Shaw JD, Sullivan K, Zesiewicz TA. Treatment of cerebellar ataxia. Neurodegener Dis Manag 2014; 4(5): 379-92.
[63] Morton SM, Bastian AJ. Can rehabilitation help ataxia? Neurology 2009; 73(22): 1818-9.
[64] Crowner BE. Cervical dystonia: Disease profile and clinical management. Phys Ther 2007; 87(11): 1511-26.
[65] Shaikh AG, Zee DS, Crawford JD, Jinnah HA. Cervical dystonia: A neural integrator disorder. Brain 2016; 139(Pt 10): 2590-9.
[66] Bashir H, Jankovic J. Treatment options for chorea. Expert Rev Neurother 2018; 18(1): 51-63.
[67] Hermann A, Walker RH. Diagnosis and treatment of chorea syndromes. Curr Neurol Neurosci Rep 2015; 15(2): 514.
[68] Bates G, Tabrizi S, Jones L, Eds. Huntington’s disease (No 64) 2014.
[69] Myers RH. Huntington’s disease genetics. NeuroRx 2004; 1(2): 255-62.
[70] Wyant KJ, Ridder AJ, Dayalu P. Huntington’s Disease-Update on Treatments. Curr Neurol Neurosci Rep 2017; 17(4): 33.
[71] Swan L, Dupont J. Multiple system atrophy. Phys Ther 1999; 79(5): 488-94.
[72] Palma JA, Norcliffe-Kaufmann L, Kaufmann H. Diagnosis of multiple system atrophy. Auton Neurosci 2018; 211: 15-25.
[73] Lance JW. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes. Adv Neurol 1986; 43: 33-55.
[74] Chokroverty S. Propriospinal myoclonus. Clin Neurosci 1995-1996; 3(4): 219-22.
[75] Shulman JM, De Jager PL, Feany MB. Parkinson’s disease: Genetics and pathogenesis. Annu Rev Pathol 2011; 6: 193-222.
[76] Hasnain M, Vieweg WV, Baron MS, Beatty-Brooks M, Fernandez A, Pandurangi AK. Pharmacological management of psychosis in elderly patients with parkinsonism. Am J Med 2009; 122(7): 614-22.
[77] Armstrong MJ. Progressive Supranuclear Palsy: an Update. Curr Neurol Neurosci Rep 2018; 18(3): 12.
[78] Barsottini OG, Felício AC, Aquino CC, Pedroso JL. Progressive supranuclear palsy: New concepts. Arq Neuropsiquiatr 2010; 68(6): 938-46.
[79] Japaridze G, Kasradze S, Maisuradze L, Popp R, Wetter T. The Restless Legs Syndrome. Georgian Med News 2018; (285): 74-81.
[80] Venkateshiah SB, Ioachimescu OC. Restless legs syndrome. Crit Care Clin 2015; 31(3): 459-72.
[81] Vijayakumar D, Jankovic J. Drug-Induced Dyskinesia, Part 2: Treatment of Tardive Dyskinesia. Drugs 2016; 76(7): 779-87.
[82] Fernandez HH, Friedman JH. Classification and treatment of tardive syndromes. Neurologist 2003; 9(1): 16-27.
[83] Efron D, Dale RC. Tics and Tourette syndrome. J Paediatr Child Health 2018; 54(10): 1148-53.
[84] Leckman JF. Tourette’s syndrome. Lancet 2002; 360(9345): 1577-86.
[85] Ferenci P. Diagnosis of Wilson disease. Handb Clin Neurol 2017; 142: 171-80.
[86] Singh S, Behari M. Wilson’s disease. J Assoc Physicians India 2003; 51: 183-90.
[87] Hardiman O, Al-Chalabi A, Chio A, et al. Amyotrophic lateral sclerosis. Nat Rev Dis Primers 2017; 3: 17071.
[88] Brown RH, Al-Chalabi A. Amyotrophic Lateral Sclerosis. N Engl J Med 2017; 377(2): 162-72.
[89] Ramchandren S. Charcot-Marie-Tooth Disease and Other Genetic Polyneuropathies. Continuum (Minneap Minn) (5,Peripheral Nerve and Motor Neuron Disorders) 2017; 23: 1360-77.
[90] Sman AD, Hackett D, Fiatarone Singh M, Fornusek C, Menezes MP, Burns J. Systematic review of exercise for Charcot-Marie-Tooth disease. J Peripher Nerv Syst 2015; 20(4): 347-62.
[91] Koch MW, Metz LM, Agrawal SM, Yong VW. Environmental factors and their regulation of immunity in multiple sclerosis. J Neurol Sci 2013; 324(1-2): 10-6.
[92] Martinelli V. Trauma, stress and multiple sclerosis. Neurol Sci 2000; 21(4)(Suppl. 2): S849-52.
[93] Carter JC, Sheehan DW, Prochoroff A, Birnkrant DJ. Muscular Dystrophies. Clin Chest Med 2018; 39(2): 377-89.
[94] Turner C, Hilton-Jones D. Myotonic dystrophy: diagnosis, management and new therapies. Curr Opin Neurol 2014; 27(5): 599-606.
[95] Gilhus NE. Myasthenia Gravis. N Engl J Med 2016; 375(26): 2570-81.
[96] Sieb JP. Myasthenia gravis: An update for the clinician. Clin Exp Immunol 2014; 175(3): 408-18.
[97] Miller ML, Shefner JM, Callen J. Diagnosis and differential diagnosis of dermatomyositis and polymyositis in adults www. uptodate. com2017.
[98] Bohan A, Peter JB. Polymyositis and dermatomyositis (second of two parts). N Engl J Med 1975; 292(8): 403-7.
[99] Watson JC, Dyck PJ. Peripheral neuropathy: A practical approach to diagnosis and symptom management. Mayo Clin Proc 2015; 90(7): 940-51.
[100] Hughes RAC. Peripheral neuropathy. BMJ 2002; 324(7335): 466-9.
[101] Dubowitz V. Ramblings in the history of spinal muscular atrophy. Neuromuscul Disord 2009; 19(1): 69-73.
[102] Nicole S, Diaz CC, Frugier T, Melki J. Spinal muscular atrophy: Recent advances and future prospects. Muscle Nerve 2002; 26(1): 4-13.
[103] Abou-Khalil BW, Gallagher MJ, Macdonald RL. Epilepsies.Bradley’s Neurology in Clinical Practice 6th ed. 2012; 1583-633.
[104] Fisher RS, Schachter SC. The postictal state: A neglected entity in the management of epilepsy. Epilepsy Behav 2000; 1(1): 52-9.
[105] Asadi-Pooya AA. Psychogenic nonepileptic seizures: A concise review. Neurol Sci 2017; 38(6): 935-40.
[106] De Clerck L, Nica A, Biraben A. Clinical aspects of seizures in the elderly. Geriatr Psychol Neuropsychiatr Vieil 2019; 17(S1): 7-12.
[107] Devinsky O, Schein A, Najjar S. Epilepsy associated with systemic autoimmune disorders. Epilepsy Curr 2013; 13(2): 62-8.
[108] Brigo F, Trinka E, Lattanzi S, Bragazzi NL, Nardone R, Martini M. A brief history of typical absence seizures - Petit mal revisited. Epilepsy Behav 2018; 80: 346-53.
[109] Pack AM. Epilepsy Overview and Revised Classification of Seizures and Epilepsies. Continuum (Minneap Minn) 2019; 25(2): 306-21.
[110] Wakai A, McCabe A, Roberts I, Schierhout G. Mannitol for acute traumatic brain injury. Cochrane Database Syst Rev 2013; 8(8)CD001049
[111] Burgess S, Abu-Laban RB, Slavik RS, Vu EN, Zed PJ. A systematic review of randomized controlled trials comparing hypertonic sodium solutions and mannitol for traumatic brain injury: Implications for emergency department management. Ann Pharmacother 2016; 50(4): 291-300.
[112] McNeill KA. Epidemiology of brain tumors. Neurol Clin 2016; 34(4): 981-98.
[113] Hadidchi S, Surento W, Lerner A, et al. Headache and brain tumor. Neuroimaging Clin N Am 2019; 29(2): 291-300.
[114] Schnurr PP, Friedman MJ, Engel CC, et al. Cognitive behavioral therapy for posttraumatic stress disorder in women: A randomized controlled trial. JAMA 2007; 297(8): 820-30.
[115] Whitfield C. Psychiatric drugs as agents of Trauma. Int J Risk Saf Med 2010; 22(4): 195-207.
[116] National Collaborating Centre for Mental Health (UK). Post-Traumatic Stress Disorder: The management of PTSD in adults and children in primary and secondary care 2005.
[117] Jonas DE, Cusack K, Forneris CA, et al. Psychological and pharmacological treatments for adults with posttraumatic stress disorder (PTSD) 2013; 92.
[118] Tharoor H, Kumar TR. Psychotic disorders including schizo- phrenia.Emergencies in psychiatry in low-and middle-income countries 2017; 25-35.
[119] Tsuang MT, Van Os J, Tandon R, et al. Attenuated psychosis syndrome in DSM-5. Schizophr Res 2013; 150(1): 31-5.
[120] Rodrigues MF, Nardi AE, Levitan M. Mindfulness in mood and anxiety disorders: A review of the literature. Trends Psychiatry Psychother 2017; 39(3): 207-15.
[121] Anthes E. Depression: A change of mind. Nature 2014; 515(7526): 185-7.
[122] Uher R, Treasure J. Brain lesions and eating disorders. J Neurol Neurosurg Psychiatry 2005; 76(6): 852-7.
[123] Romanos GE, Javed F, Romanos EB, Williams RC. Oro-facial manifestations in patients with eating disorders. Appetite 2012; 59(2): 499-504.
[124] Tyrer P, Reed GM, Crawford MJ. Classification, assessment, prevalence, and effect of personality disorder. Lancet 2015; 385(9969): 717-26.
[125] Magnavita JJ. EdHandbook of personality disorders: Theory and practice 2004.
[126] Başar E, Güntekin B. A review of brain oscillations in cognitive disorders and the role of neurotransmitters. Brain Res 2008; 1235: 172-93.
[127] Hardy JA, Higgins GA. Alzheimer’s disease: The amyloid cascade hypothesis. Science 1992; 256(5054): 184-5.
[128] Cipriani G, Dolciotti C, Picchi L, Bonuccelli U. Alzheimer and his disease: A brief history. Neurol Sci 2011; 32(2): 275-9.
[129] Jankovic J. Parkinson’s disease: Clinical features and diagnosis. J Neurol Neurosurg Psychiatry 2008; 79(4): 368-76.
[130] Alzheimer’s Association. Alzheimer’s disease facts and figures. Alzheimers Dement 2017; 13(4): 325-73.
[131] Dubois B, Hampel H, Feldman HH, et al. Proceedings of the meeting of the International Working Group (IWG) and the American Alzheimer’s Association on “The Preclinical State of AD”; July 23, 2015; Washington DC, USA. Preclinical Alzheimer’s disease: Definition, natural history, and diagnostic criteria. Alzheimers Dement 2016; 12(3): 292-323.
[132] Jost BC, Grossberg GT. The evolution of psychiatric symptoms in Alzheimer’s disease: A natural history study. J Am Geriatr Soc 1996; 44(9): 1078-81.
[133] Calne DB, Langston JW. Aetiology of Parkinson's disease. Lancet 1983; 2(8365-66): 1457-9.
[134] McCall B. Young-onset Parkinson’s disease: A guide to care and support. Nurs Times 2003; 99(30): 28-31.
[135] Sveinbjornsdottir S. The clinical symptoms of Parkinson’s disease. J Neurochem 2016; 139(Suppl. 1): 318-24.
[136] Chesebro B. Introduction to the transmissible spongiform encephal- opathies or prion diseases. Br Med Bull 2003; 66: 1-20.
[137] Goldmann W. PrP genetics in ruminant transmissible spongiform encephalopathies. Vet Res 2008; 39(4): 30.
[138] Castle AR, Gill AC. Physiological functions of the cellular prion protein. Front Mol Biosci 2017; 4: 19.
[139] Brown P. The risk of bovine spongiform encephalopathy (‘mad cow disease’) to human health. JAMA 1997; 278(12): 1008-11.
[140] Vonsattel JP, DiFiglia M. Huntington disease. J Neuropathol Exp Neurol 1998; 57(5): 369-84.
[141] Andrew SE, Goldberg YP, Kremer B, et al. Huntington disease without CAG expansion: phenocopies or errors in assignment? Am J Hum Genet 1994; 54(5): 852-63.
[142] Brower MC, Price BH. Neuropsychiatry of frontal lobe dysfunction in violent and criminal behaviour: A critical review. J Neurol Neurosurg Psychiatry 2001; 71(6): 720-6.
[143] Berrios GE, Marková IS. The concept of neuropsychiatry: A historical overview. J Psychosom Res 2002; 53(2): 629-38.
[144] Kas MJ, Penninx B, Sommer B, Serretti A, Arango C, Marston H. A quantitative approach to neuropsychiatry: The why and the how. Neurosci Biobehav Rev 2019; 97: 3-9.
[145] Autry AE, Monteggia LM. Brain-derived neurotrophic factor and neuropsychiatric disorders. Pharmacol Rev 2012; 64(2): 238-58.
[146] Cummings JL, Mega MS. Neuropsychiatry and behavioral neuroscience 2003.
[147] Rapoport J, Chavez A, Greenstein D, Addington A, Gogtay N. Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited. J Am Acad Child Adolesc Psychiatry 2009; 48(1): 10-8.
[148] Cornblatt BA, Keilp JG. Impaired attention, genetics, and the pathophysiology of schizophrenia. Schizophr Bull 1994; 20(1): 31-46.
[149] Uhl GR, Grow RW. The burden of complex genetics in brain disorders. Arch Gen Psychiatry 2004; 61(3): 223-9.
[150] Cannon JR, Greenamyre JT. The role of environmental exposures in neurodegeneration and neurodegenerative diseases. Toxicol Sci 2011; 124(2): 225-50.
[151] Hussain R, Zubair H, Pursell S, Shahab M. Neurodegenerative Diseases: Regenerative Mechanisms and Novel Therapeutic Approaches. Brain Sci 2018; 8(9): 177.
[152] Prusiner SB. Shattuck lecture--neurodegenerative diseases and prions. N Engl J Med 2001; 344(20): 1516-26.
[153] Goedert M. Alpha-synuclein and neurodegenerative diseases. Nat Rev Neurosci 2001; 2(7): 492-501.
[154] Beal MF. Mitochondrial dysfunction in neurodegenerative diseases. Biochim Biophys Acta 1998; 1366(1-2): 211-23.
[155] Taber KH, Hurley RA, Yudofsky SC. Diagnosis and treatment of neuropsychiatric disorders. Annu Rev Med 2010; 61: 121-33.
[156] Vadakkan KI. Neurodegenerative disorders share common features of “loss of function” states of a proposed mechanism of nervous system functions. Biomed Pharmacother 2016; 83: 412-30.
[157] Hervás R, Oroz J, Galera-Prat A, et al. Common features at the start of the neurodegeneration cascade. PLoS Biol 2012; 10(5)e1001335
[158] Brookmeyer R, Johnson E, Ziegler-Graham K, Arrighi HM. Forecasting the global burden of Alzheimer’s disease. Alzheimers Dement 2007; 3(3): 186-91.
[159] Datta G, Colasanti A, Rabiner EA, et al. Neuroinflammation and its relationship to changes in brain volume and white matter lesions in multiple sclerosis. Brain 2017; 140(11): 2927-38.
[160] Brown RC, Lockwood AH, Sonawane BR. Neurodegenerative diseases: An overview of environmental risk factors. Environ Health Perspect 2005; 113(9): 1250-6.
[161] Chin-Chan M, Navarro-Yepes J, Quintanilla-Vega B. Environmental pollutants as risk factors for neurodegenerative disorders: Alzheimer and Parkinson diseases. Front Cell Neurosci 2015; 9: 124.
[162] Uher R. Gene-environment interactions in severe mental illness. Front Psychiatry 2014; 5: 48.
[163] Faraone SV, Larsson H. Genetics of attention deficit hyperactivity disorder. Mol Psychiatry 2019; 24(4): 562-75.
[164] Franke B, Faraone SV, Asherson P, et al. International Multicentre persistent ADHD CollaboraTion. The genetics of attention deficit/hyperactivity disorder in adults, a review. Mol Psychiatry 2012; 17(10): 960-87.
[165] Kozlowski H, Luczkowski M, Remelli M, Valensin D. Copper, zinc and iron in neurodegenerative diseases (Alzheimer’s, Parkinson’s and prion diseases). Coord Chem Rev 2012; 256(19-20): 2129-41.
[166] Barnham KJ, Bush AI. Metals in Alzheimer’s and Parkinson’s diseases. Curr Opin Chem Biol 2008; 12(2): 222-8.
[167] Jokanović M. Neurotoxic effects of organophosphorus pesticides and possible association with neurodegenerative diseases in man: A review. Toxicology 2018; 410: 125-31.
[168] Uversky VN. Neurotoxicant-induced animal models of Parkinson’s disease: understanding the role of rotenone, maneb and paraquat in neurodegeneration. Cell Tissue Res 2004; 318(1): 225-41.
[169] Caudle WM, Guillot TS, Lazo CR, Miller GW. Industrial toxicants and Parkinson’s disease. Neurotoxicology 2012; 33(2): 178-88.
[170] Gowthaman R, Gowthaman N, Rajangam MK, Srinivasan K. Database of neurodegenerative disorders. Bioinformation 2007; 2(4): 153-4.
[171] Xie SX, Baek Y, Grossman M, et al. Building an integrated neurodegenerative disease database at an academic health center. Alzheimers Dement 2011; 7(4): e84-93.
[172] Kandale VV, Mujawar SN, Welasly PJ, et al. Development of integrated database of neurodegenerative diseases (IDND). Rev Res 2013; 2(9): 1-5.
[173] Lill CM, Roehr JT, McQueen MB, et al. Comprehensive research synopsis and systematic meta-analyses in Parkinson’s disease genetics: The PDGene database. PLoS Genet 2012; 8(3)e1002548
[174] Zhang DF, Fan Y, Xu M, et al. Complement C7 is a novel risk gene for Alzheimer’s disease in Han Chinese. Natl Sci Rev 2019; 6(2): 257-74.
[175] Chang SH, Gao L, Li Z, Zhang WN, Du Y, Wang J. BDgene: A genetic database for bipolar disorder and its overlap with schizophrenia and major depressive disorder. Biol Psychiatry 2013; 74(10): 727-33.
[176] Wu Y, Li X, Liu J, Luo XJ, Yao YG. SZDB2.0: An updated comprehensive resource for schizophrenia research. Hum Genet 2020.
[177] Jennings CG, Landman R, Zhou Y, et al. Opportunities and challenges in modeling human brain disorders in transgenic primates. Nat Neurosci 2016; 19(9): 1123-30.
[178] Buffalo EA, Movshon JA, Wurtz RH. From basic brain research to treating human brain disorders. Proc Natl Acad Sci USA 2019; 116(52): 26167-72.
[179] Harrington AJ, Hamamichi S, Caldwell GA, et al. C. elegans as a model organism to investigate molecular pathways involved with Parkinson's disease. Dev Dyn 2010; 239(5): 1282-95.
[180] Alexander AG, Marfil V, Li C. Use of Caenorhabditis elegans as a model to study Alzheimer’s disease and other neurodegenerative diseases. Front Genet 2014; 5: 279.
[181] Voisine C, Hart AC. Caenorhabditis elegans as a model system for triplet repeat diseases.Trinucleotide Repeat Protocols 2004; 141-60.
[182] Cauchi RJ, van den Heuvel M. The fly as a model for neurodegenerative diseases: Is it worth the jump? Neurodegener Dis 2006; 3(6): 338-56.
[183] Sang TK, Jackson GR. Drosophila models of neurodegenerative disease. NeuroRx 2005; 2(3): 438-46.
[184] Bilen J, Bonini NM. Drosophila as a model for human neurodegenerative disease. Annu Rev Genet 2005; 39: 153-71.
[185] Xi Y, Noble S, Ekker M. Modeling neurodegeneration in zebrafish. Curr Neurol Neurosci Rep 2011; 11(3): 274-82.
[186] Best JD, Alderton WK. Zebrafish: An in vivo model for the study of neurological diseases. Neuropsychiatr Dis Treat 2008; 4(3): 567-76.
[187] Leung C, Jia Z. Mouse genetic models of human brain disorders. Front Gene 2016; 7(40)
[188] Tayebati SK, Tomassoni D, Amenta F. Spontaneously hypertensive rat as a model of vascular brain disorder: Microanatomy, neurochemistry and behavior. J Neurol Sci 2012; 322(1-2): 241-9.
[189] Lo Bianco C, Ridet JL, Schneider BL, Deglon N, Aebischer P. α -Synucleinopathy and selective dopaminergic neuron loss in a rat lentiviral-based model of Parkinson’s disease. Proc Natl Acad Sci USA 2002; 99(16): 10813-8.
[190] Gieling ET, Schuurman T, Nordquist RE, et al. The pig as a model animal for studying cognition and neurobehavioral disorders.Mol Func Mod Neuropsych 2011; 359-83.
[191] Lind NM, Moustgaard A, Jelsing J, Vajta G, Cumming P, Hansen AK. The use of pigs in neuroscience: Modeling brain disorders. Neurosci Biobehav Rev 2007; 31(5): 728-51.
[192] Fan N, Lai L. Genetically modified pig models for human diseases. J Genet Genomics 2013; 40(2): 67-73.
[193] Cai DC, Wang Z, Bo T, et al. MECP2 duplication causes aberrant GABA pathways, circuits and behaviors in transgenic monkeys: Neural mappings to patients with autism. J Neurosci 2020; 40(19): 3799-814.
[194] Li X, Yang W, Li X, et al. Alpha-synuclein oligomerization and dopaminergic degeneration occur synchronously in the brain and colon of MPTP-intoxicated parkinsonian monkeys. Neurosci Lett 2020; 716: 134640.
[195] Ke Q, Li W, Lai X, et al. TALEN-based generation of a cynomolgus monkey disease model for human microcephaly. Cell Res 2016; 26(9): 1048-61.
[196] Elfenbein HA, Rosen RF, Stephens SL, et al. Cerebral ß-amyloid angiopathy in aged squirrel monkeys 2007.
[197] Barraud Q, Lambrecq V, Forni C, et al. Sleep disorders in Parkinson’s disease: The contribution of the MPTP non-human primate model. Exp Neurol 2009; 219(2): 574-82.
[198] Berg D. Biomarkers for the early detection of Parkinson’s and Alzheimer’s disease. Neurodegener Dis 2008; 5(3-4): 133-6.
[199] Shulman JM, De Jager PL. Evidence for a common pathway linking neurodegenerative diseases. Nat Genet 2009; 41(12): 1261-2.
[200] Kauwe JS, Cruchaga C, Mayo K, et al. Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition. Proc Natl Acad Sci USA 2008; 105(23): 8050-4.
[201] Silva GA. Nanotechnology approaches to crossing the blood-brain barrier and drug delivery to the CNS. BMC Neurosci 2008; 9(Suppl. 3): S4.
[202] Krol S, Macrez R, Docagne F, et al. Therapeutic benefits from nanoparticles: the potential significance of nanoscience in diseases with compromise to the blood brain barrier. Chem Rev 2013; 113(3): 1877-903.
[203] Brigger I, Morizet J, Aubert G, et al. Poly(ethylene glycol)-coated hexadecylcyanoacrylate nanospheres display a combined effect for brain tumor targeting. J Pharmacol Exp Ther 2002; 303(3): 928-36.
[204] Kreuter J. Drug delivery to the central nervous system by polymeric nanoparticles: What do we know? Adv Drug Deliv Rev 2014; 71: 2-14.