Neurological Disorders

Neurological Disorders

A neurological disorder is one that affects the body's nervous system, i.e. the brain, the spinal cord, and the nerves that lead to and from them. Neurological disorders are quite widespread- according to a recent survey of the World Health Organization over 1 billion people suffer from neurological problems and can afflict people of any age.

There are many and quite diverse - factors that may lead to a neurological disorder as, for example, congenital abnormalities, brain or spinal cord injuries, malnutrition, infections, immune system problems, cardiovascular complications, as well as social stigma and discrimination. In some disorders, the nervous cells responsible for the production of dopamine and other substances are slowly destroyed. This process, together with some infections, has been linked to neurological conditions. Other risk factors are heredity, age, gender, reduced levels of estrogen, exposure to different chemicals, and exposure to chemicals during fetal developments.

Symptoms of neurological conditions are rigid muscles, tremors, slow motion, difficulty swallowing, numbness, and intermittent twitching. Other symptoms include inability to speak clearly, lack of balance and coordination, and lost ability for automatic movements, e.g. blinking. In some cases, neurological disorders result in dementia.

Neurological disorders often cause mild to severe depression. They are typically slow to develop and the onset is marked by mild symptoms. Patients are often doing household chores, cooking, or driving, and symptoms can cause accidents. With disease progression, patients are exposed to higher risks of depression. If they lose independence, depression may become especially severe.

Most neurological diseases are difficult to treat. Physical therapy is typically prescribed to retain physical dexterity. Medications such as anticholinergics, selegiline, Levopoda, amantadine, and dopamine agonists may help during various phases of the disease. Surgery is an option only for patients who can withstand surgical intervention. The surgical procedure involves the destruction of tiny amounts of brain tissue in the area affected by the disease. Another procedure involves stimulation of various brain parts. Today surgical treatment is a less common practice, with medications preferred by the physicians. Some of the most common disorders resulting from these factors are: Alzheimer's disease, Parkinson's disease, Epilepsy, and Alper's syndrome, among others.

Alzheimer's disease

Alzheimer's is a particularly acute form of dementia. It is an incurable, degenerative, and terminal disease that is diagnosed in predominantly older people (over 65 years of age). Its most likely cause are the senile plaques and neurofibrillary tangles that accumulate in the brain with time. In its early stage, the disease is characterized by memory loss, e.g. the inability or difficulty in remembering recently learned information. As it progresses, other symptoms of the disease will appear: confusion, mood swings, irritability, aggression, language breakdown, and the overall withdrawal of the patient.

At present, there is no surefire measure to avoid Alzheimer's disease, but studies have shown that a person who regularly engages in intellectual activities (reading, playing board games, completing crosswords, etc.), plays a musical instrument, and actively interacts with other people, is less likely to be affected by it.

Parkinson's disease

This is a degenerative disorder that often impairs the patient's motor skills and speech. The most common cause of the disease is some form of head trauma although toxicity occasioned by heavy drug intake may also prove a highly harmful factor. Parkinson's disease is rather conspicuous as it is often accompanied by limb tremors and postural instability. It is an incurable disorder, but its symptoms can be greatly alleviated via a well-balanced combination of healthy diet, physiotherapy, exercise, and medication.

Epilepsy

This is a disease characterized by chronic, unprovoked seizures of varying severity. More than 50 million people worldwide suffer from this epilepsy, the majority being small children and adults over the age of 65 years. About 70 percent of the cases can be successfully controlled with the appropriate medication and/ or surgical intervention.

Alpers' Syndrome

This disease affects infants and small children up to five years old. Its first symptoms include seizures and inability to meet the development standards for the particular age. As the disease advances, the child becomes afflicted with mental retardation, spasticity (limb stiffness), and progressive dementia. Optic atrophy that often leads to blindness may also occur.

There is no cure for Alpers' syndrome, although some of the symptoms may be treated separately. Anticonvulsants can be used to decrease seizure intensity, and physical therapy can help relieve the stiffness of the limbs.

Absence of the Septum Pellucidum
Acid Lipase Disease
Acute Disseminated Encephalomyelitis
Adrenoleukodystrophy
Agenesis of the Corpus Callosum
Agnosia
Aicardi Syndrome
Aicardi-Goutieres Syndrome Disorder
Alexander Disease
Alpers' Disease
Alternating Hemiplegia
Alzheimer's Disease
Amyotrophic Lateral Sclerosis
Anencephaly
Angelman Syndrome
Antiphospholipid Syndrome
Aphasia
Apraxia
Arachnoid Cysts
Arachnoiditis
Arteriovenous Malformation
Asperger Syndrome
Ataxia Telangiectasia
Ataxias and Cerebellar or Spinocerebellar Degeneration
Atrial Fibrillation and Stroke
Attention Deficit-Hyperactivity Disorder
Autism
Back Pain
Barth Syndrome
Batten Disease
Behcet's Disease
Bell's Palsy
Benign Essential Blepharospasm
Binswanger's Disease
Brachial Plexus Injuries
Brain and Spinal Tumors
Brown-Sequard Syndrome
CADASIL
Canavan Disease
Carpal Tunnel Syndrome
Central Cord Syndrome
Central Pain Syndrome
Central Pontine Myelinolysis
Cephalic Disorders
Cerebellar Degeneration
Cerebellar Hypoplasia
Cerebral Aneurysm
Cerebral Arteriosclerosis
Cerebral Atrophy
Cerebral Cavernous Malformation
Cerebral Hypoxia
Cerebral Palsy
Cerebro-Oculo-Facio-Skeletal Syndrome
Charcot-Marie-Tooth Disease
Chiari Malformation
Chorea
Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
Chronic Pain
Coffin Lowry Syndrome
Colpocephaly
Coma
Complex Regional Pain Syndrome
Congenital Myasthenia
Congenital Myopathy
Corticobasal Degeneration
Craniosynostosis
Creutzfeldt-Jakob Disease
Cushing's Syndrome
Dandy-Walker Syndrome
Deep Brain Stimulation for Parkinson's Disease
Dementia
Dementia With Lewy Bodies
Dermatomyositis
Developmental Dyspraxia
Diabetic Neuropathy
Dravet Syndrome
Dysautonomia
Dysgraphia
Dyslexia
Dyssynergia Cerebellaris Myoclonica
Dystonias
Empty Sella Syndrome
Encephalitis Lethargica
Encephaloceles
Encephalopathy
Epilepsy
Erb-Duchenne and Dejerine-Klumpke Palsies
Essential Tremor
Fabry Disease
Fahr's Syndrome
Familial Periodic Paralyses
Farber's Disease
Febrile Seizures
Fibromuscular Dysplasia
Foot Drop
Friedreich's Ataxia
Frontotemporal Dementia
Gangliosidoses
Gaucher's Disease
Gerstmann's Syndrome
Gerstmann-Straussler-Scheinker Disease
Giant Axonal Neuropathy
Glossopharyngeal Neuralgia
Guillain-Barre Syndrome
Headache
Hemicrania Continua
Hemifacial Spasm
Hereditary Neuropathies
Hereditary Spastic Paraplegia
Herpes Zoster Oticus
Holmes-Adie syndrome
Holoprosencephaly
Huntington's Disease
Hydranencephaly
Hydrocephalus
Hydromyelia
Hypersomnia
Hypertonia
Hypotonia
Inclusion Body Myositis
Incontinentia Pigmenti
Infantile Neuroaxonal Dystrophy
Infantile Refsum Disease
Infantile Spasms
Inflammatory Myopathies
Iniencephaly
Isaac's Syndrome
Joubert Syndrome
Kearns-Sayre Syndrome
Kennedy's Disease
Kleine-Levin Syndrome
Klippel-Feil Syndrome
Klippel-Trenaunay Syndrome (KTS)
Klüver-Bucy Syndrome
Krabbe Disease
Kuru
Lambert-Eaton Myasthenic Syndrome
Landau-Kleffner Syndrome
Learning Disabilities
Leigh's Disease
Lennox-Gastaut Syndrome
Lesch-Nyhan Syndrome
Leukodystrophy
Lipid Storage Diseases
Lipoid Proteinosis
Lissencephaly
Locked-In Syndrome
Machado-Joseph Disease
Megalencephaly
Melkersson-Rosenthal Syndrome
Meningitis and Encephalitis
Menkes Disease
Meralgia Paresthetica
Metachromatic Leukodystrophy
Microcephaly
Migraine
Miller Fisher Syndrome
Mitochondrial Myopathies
Moebius Syndrome
Monomelic Amyotrophy
Motor Neuron Diseases
Moyamoya Disease
Mucolipidoses
Mucopolysaccharidoses
Multi-Infarct Dementia
Multifocal Motor Neuropathy
Multiple Sclerosis
Multiple System Atrophy
Multiple System Atrophy with Orthostatic Hypotension
Muscular Dystrophy
Myasthenia Gravis
Myoclonus
Myopathy
Myotonia
Myotonia Congenita
Narcolepsy
Neuroacanthocytosis
Neurodegeneration with Brain Iron Accumulation
Neurofibromatosis
Neuroleptic Malignant Syndrome
Neurological Complications of AIDS
Neurological Complications Of Lyme Disease
Neurological Consequences of Cytomegalovirus Infection
Neurological Sequelae Of Lupus
Neuromyelitis Optica
Neuronal Migration Disorders
Neurosarcoidosis
Neurosyphilis
Neurotoxicity
Niemann-Pick Disease
Normal Pressure Hydrocephalus
Occipital Neuralgia
Ohtahara Syndrome
Olivopontocerebellar Atrophy
Opsoclonus Myoclonus
Orthostatic Hypotension
Paraneoplastic Syndromes
Paresthesia
Parkinson's Disease
Paroxysmal Choreoathetosis
Paroxysmal Hemicrania
Parry-Romberg
Pelizaeus-Merzbacher Disease
Peripheral Neuropathy
Periventricular Leukomalacia
Pervasive Developmental Disorders
Pinched Nerve
Piriformis Syndrome
Pituitary Tumors
Polymyositis
Pompe Disease
Porencephaly
Post-Polio Syndrome
Postural Tachycardia Syndrome
Primary Lateral Sclerosis
Progressive Multifocal Leukoencephalopathy
Progressive Supranuclear Palsy
Prosopagnosia
Pseudotumor Cerebri
Rasmussen's Encephalitis
Refsum Disease
Repetitive Motion Disorders
Restless Legs Syndrome
Rett Syndrome
Reye's Syndrome
Sandhoff Disease
Schilder's Disease
Schizencephaly
Septo-Optic Dysplasia
Shaken Baby Syndrome
Shingles
Sjögren's Syndrome
Sleep Apnea
Sotos Syndrome
Spasticity
Spina Bifida
Spinal Cord Infarction
Spinal Cord Injury
Spinal Muscular Atrophy
Stiff-Person Syndrome
Striatonigral Degeneration
Stroke
Sturge-Weber Syndrome
Subacute Sclerosing Panencephalitis
SUNCT Headache
Swallowing Disorders
Sydenham Chorea
Syncope
Syringomyelia
Tabes Dorsalis
Tardive Dyskinesia
Tarlov Cysts
Tay-Sachs Disease
Tethered Spinal Cord Syndrome
Thoracic Outlet Syndrome
Thyrotoxic Myopathy
Todd's Paralysis
Tourette Syndrome
Transient Ischemic Attack
Transmissible Spongiform Encephalopathies
Transverse Myelitis
Traumatic Brain Injury
Tremor
Trigeminal Neuralgia
Tropical Spastic Paraparesis
Troyer Syndrome
Tuberous Sclerosis
Vasculitis Syndromes of the Central and Peripheral Nervous Systems
Von Hippel-Lindau Disease (VHL)
Wallenberg's Syndrome
Wernicke-Korsakoff Syndrome
Whiplash
Whipple's Disease
Williams Syndrome
Wilson's Disease
Zellweger Syndrome


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