Treatment/Cure: No known cure but treatment is symptomatic. Huntington's disease. Cardiomyopathy dilated with conduction defect type 2. Cranioencephalic disorders. According to the National Institute of Neurological Disorders and Stroke, damage to the brain and the neurological system can wreak havoc on our fragile bodies. Lewy body disease. … Amyotrophic Lateral Sclerosis (ALS) Anencephaly. Acrofacial dysostosis Catania type. Awareness: International Rett Syndrome Foundation has an awareness week in October, Treatment/Cure: No known cure, but treatment is symptomatic. In other words, the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscles. The incubation period can be upwards of 50 years, so all we can do is hope that this disease stays in the past. Parkinson's disease. Creutzfeldt-Jakob disease (CJD) is an extremely rare degenerative brain disorder (i.e., spongiform encephalopathy) characterized by sudden development of rapidly progressive neurological and neuromuscular symptoms. Epilepsy and Seizures. Medications for Neurological Disorders Medication List; About Neurological Disorders. Some neurological disorders in children develop due to postnatal infections. 1 There are a variety of symptoms categorized in three stages that provide a general basis for diagnosing individuals with LS. Cardiomyopathy cataract hip spine disease. Appearing in infancy, this condition is not a degenerative disorder and is often confused with Autism or Cerebral Palsy. Symptoms include weakness and wasting of muscles of the hands, forearms, … Causes of neurological disorders include genetics, injury and environment with symptoms ranging in severity from curable, to controllable, to life-threatening. E: Disease is an autoimmune response triggered by a specific environmental factor. Brain Tumors. Amyotrophic lateral sclerosis. Agnosia is a condition where you are unable to properly perceive objects. With symptom onset, affected : Josef Gerstmann, Ernst Sträussler and Ilya Scheinker, Awareness: The CJD Foundation helps raise awareness of Prion diseases, Treatment/Cure: No treatments or cures other than symptomatic. Drugs used to treat Neurological Disorders. : Hans Gerhard Creutzfeldt, Awareness: Creutzfeldt-Jakob Disease Foundation, Inc – November 12th, Treatment/Cure: Supportive and symptomatic therapy can help. Absence of septum pellucidum. Kleine-Levin Syndrome This rare form of Alzheimer's disease usually occurs between the ages of 30 and 60, and individuals with a family history of FAD have a 50 percent chance of developing dementia. Cephalic Disorders. Who discovered it? : An international team of researchers, Awareness: September 30th is Microcephaly Awareness Day, Treatment/Cure: Therapy can be helpful but there is no known treatment or cure. Other symptoms include difficulty walking and loss of control of bodily movement. Who discovered it? Seizures. Cardiomyopathy and deafness due to tRNA lysine gene mutation. This rare neurological disease is said to be like a spelling mistake in the genes, resulting in mutations, with less than 50 cases of Cantu Syndrome having been described in medical literature. Cerebellar Degeneration. : Daniel Carleton Gajdusek, Treatment/Cure: None, other than ceasing to commit cannibalism. Angelman Syndrome. Acrocallosal syndrome, Schinzel type. Abetalipoproteinemia. Aceruloplasminemia. The International Rett Syndrome Foundation has a PSA that they play on TV and Radio and it has received over 300 million impressions, which helps them to connect to more families dealing with Rett, and to raise more awareness. Agnosia. Inclusion on this list does not serve as official recognition by the NIH that a disease is rare. F: Disease is only caused by autoimmunity in only a fraction of those who suffer from it. For the latest updates on COVID-19, click or touch here. Read on to learn more about the ten rarest brain diseases from around the world, and be thankful for every day that you wake up without them. Acrofacial dysostosis Rodriguez type. Some are inherited, some are caused by exposure, and others are both. : Dr. Van der Knaap and his colleagues. Rare Brain Disorders. It affects 2 to 3% of children with neuroblastoma. RPI Deficiency is the rarest brain disease in the world, there are only 3 known cases historically, where the patients have what is called diffuse white matter abnormalities. https://en.wikipedia.org/wiki/List_of_neurological_conditions_and_disorders Rett Syndrome occurs in approximately 1 in every 10,000 births. Disorders affecting spinal nerves, but not directly affecting the cord, cause sensory or motor abnormalities or both only in the areas supplied by the affected spinal nerves. Anti-GBM/Anti-TBM nephritis. It is an extremely rare condition, affecting as few as 1 in 10,000,000 people per year. ABri amyloidosis. Anxiety Disorders (Types: Generalized Anxiety Disorder, Panic Disorder, Phobia-Related Disorders) Aphasia. Degenerative nerve diseases include. The main symptoms include excessive hair growth and distinctive, exaggerated facial features like thick eyebrows, with some patients exhibiting developmental delays. Overview. Throughout strategic decision making, the patient perspective guides our process. People with an autonomic disorder have trouble regulating one or more of these systems, which can result in fainting, lightheadedness, fluctuating blood pressure, and other symptoms. Alzheimer's disease. Get the latest research information from NIH: https://www.nih.gov/coronavirus (link is external), If you have problems viewing PDF files, download the latest version of Adobe Reader, For language access assistance, contact the NCATS Public Information Officer, Genetic and Rare Diseases Information Center (GARD) - PO Box 8126, Gaithersburg, MD 20898-8126 - Toll-free: 1-888-205-2311, expand submenu for Find Diseases By Category, expand submenu for Patients, Families and Friends, expand submenu for Healthcare Professionals, Office of Rare Disease Research Facebook Page, Office of Rare Disease Research on Twitter, U.S. Department of Health & Human Services, Caring for Your Patient with a Rare Disease, Preguntas Más Frecuentes Sobre Enfermedades Raras, Como Encontrar un Especialista en su Enfermedad, Consejos Para una Condición no Diagnosticada, Consejos Para Obtener Ayuda Financiera Para Una Enfermedad, Preguntas Más Frecuentes Sobre los Trastornos Cromosómicos, 2-methylbutyryl-CoA dehydrogenase deficiency, 3-alpha hydroxyacyl-CoA dehydrogenase deficiency, 6-pyruvoyl-tetrahydropterin synthase deficiency, Adenosine monophosphate deaminase 1 deficiency, Alaninuria with microcephaly, dwarfism, enamel hypoplasia and diabetes mellitus, Alopecia epilepsy oligophrenia syndrome of Moynahan, Alopecia, epilepsy, pyorrhea, mental subnormality, Alopecia-contractures-dwarfism-intellectual disability syndrome, Alopecia-intellectual disability syndrome, Alpha-ketoglutarate dehydrogenase deficiency, Alpha-thalassemia x-linked intellectual disability syndrome, Early-onset, autosomal dominant Alzheimer disease, Alzheimer's disease without neurofibrillary tangles, Aminolevulinate dehydratase deficiency porphyria, Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1, Anemia sideroblastic and spinocerebellar ataxia, Aniridia - ptosis - intellectual disability - familial obesity, Aniridia renal agenesis psychomotor retardation, Aortic arch anomaly - peculiar facies - intellectual disability, Aromatic L-amino acid decarboxylase deficiency, Arthrogryposis multiplex congenita, distal, X-linked, Arthrogryposis renal dysfunction cholestasis syndrome, Arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay, Ataxia - hypogonadism - choroidal dystrophy, Autosomal dominant centronuclear myopathy, Autosomal dominant cerebellar ataxia, deafness, and narcolepsy, Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons, Autosomal dominant deafness-onychodystrophy syndrome, Autosomal dominant intermediate Charcot-Marie-Tooth, Autosomal dominant leukodystrophy with autonomic disease, Autosomal dominant neuronal ceroid lipofuscinosis 4B, Autosomal dominant nocturnal frontal lobe epilepsy, Autosomal dominant non-syndromic intellectual disability, Autosomal dominant optic atrophy plus syndrome, Autosomal dominant partial epilepsy with auditory features, Autosomal dominant spinal muscular atrophy, lower extremity-predominant 1, Autosomal recessive axonal neuropathy with neuromyotonia, Autosomal recessive centronuclear myopathy, Autosomal recessive Charcot-Marie-Tooth disease with hoarseness, Autosomal recessive intermediate Charcot-Marie-Tooth disease, Autosomal recessive juvenile Parkinson disease, Autosomal recessive spastic paraplegia type 49, Autosomal recessive spinocerebellar ataxia 9, Behavioral variant of frontotemporal dementia, Benign familial neonatal-infantile seizures, Beta-Propeller Protein-Associated Neurodegeneration, Bilateral parasagittal parieto-occipital polymicrogyria, Biotin-thiamine-responsive basal ganglia disease, Brachydactyly-mesomelia-intellectual disability-heart defects syndrome, Brain dopamine-serotonin vesicular transport disease, Bullous dystrophy hereditary macular type, Camptodactyly arthropathy coxa vara pericarditis syndrome, Cerebellar ataxia and hypogonadotropic hypogonadism, Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss, Cerebellar hypoplasia tapetoretinal degeneration, Cerebellar hypoplasia with endosteal sclerosis, Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy, Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome, Cerebral sclerosis similar to Pelizaeus-Merzbacher disease, Cervical hypertrichosis peripheral neuropathy, Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids, Chronic progressive external ophthalmoplegia, Cleft palate short stature vertebral anomalies, COASY Protein-Associated Neurodegeneration, Congenital central hypoventilation syndrome, Congenital fibrosis of extraocular muscles, Congenital generalized lipodystrophy type 4, Congenital insensitivity to pain with anhidrosis, Congenital intrauterine infection-like syndrome, Congenital myasthenic syndrome with episodic apnea, Continuous spike-wave during slow sleep syndrome, Convulsions, benign familial infantile, 1, Corpus callosum agenesis double urinary collecting, Cortical blindness-intellectual disability-polydactyly syndrome, Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation, Cyprus facial neuromusculoskeletal syndrome, Dandy-Walker cyst with Renal-Hepatic-Pancreatic dysplasia, Dandy-Walker like malformation with atrioventricular septal defect, Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures, Dandy-Walker malformation with postaxial polydactyly, Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus, Deafness, dystonia, and cerebral hypomyelination, Dihydrolipoamide dehydrogenase deficiency, Dyskeratosis congenita autosomal dominant, Dyskeratosis congenita autosomal recessive, Early infantile epileptic encephalopathy 25, Early-onset parkinsonism-intellectual disability syndrome, Eosinophilic granulomatosis with polyangiitis, Epidermolysa bullosa simplex with muscular dystrophy, Epiphyseal dysplasia hearing loss dysmorphism, Facial onset sensory and motor neuronopathy, Fallot complex with severe mental and growth retardation, Familial congenital palsy of trochlear nerve, Familial encephalopathy with neuroserpin inclusion bodies, Familial focal epilepsy with variable foci, Familial hemophagocytic lymphohistiocytosis, Familial infantile convulsions and paroxysmal choreoathetosis, Fatty acid hydroxylase-associated neurodegeneration, FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome, Febrile infection-related epilepsy syndrome, Gamma aminobutyric acid transaminase deficiency, Glucose transporter type 1 deficiency syndrome, GOSR2-related progressive myoclonus ataxia, Guanidinoacetate methyltransferase deficiency, Hair defect-photosensitivity-intellectual disability syndrome, Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome, Hereditary diffuse leukoencephalopathy with spheroids, Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis, Hereditary hemorrhagic telangiectasia type 2, Hereditary hemorrhagic telangiectasia type 3, Hereditary hemorrhagic telangiectasia type 4, Hereditary motor and sensory neuropathy type 5, Hereditary neuropathy with liability to pressure palsies, Hereditary proximal myopathy with early respiratory failure, Hereditary sensorimotor neuropathy with hyperelastic skin, Hereditary sensory and autonomic neuropathy type 1E, Hereditary sensory and autonomic neuropathy type 2, Hereditary sensory and autonomic neuropathy type 7, Hereditary sensory and autonomic neuropathy type V, Horizontal gaze palsy with progressive scoliosis, HTLV-1 associated myelopathy/tropical spastic paraparesis, Hydrocephalus due to congenital stenosis of aqueduct of sylvius, Hydrocephalus-cleft palate-joint contractures syndrome, Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency, Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency, Hyperphenylalaninemia due to dehydratase deficiency, Hypertrophic neuropathy of Dejerine-Sottas, Hypomyelination with atrophy of basal ganglia and cerebellum, Hypoparathyroidism-intellectual disability-dysmorphism syndrome, Hypospadias-intellectual disability, Goldblatt type syndrome, Ichthyosis alopecia eclabion ectropion mental retardation, Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia, Infantile cerebellar retinal degeneration, Infantile choroidocerebral calcification syndrome, Infantile-onset ascending hereditary spastic paralysis, Intellectual deficit - short stature - hypertelorism, Intellectual disability - athetosis - microphthalmia, Intellectual disability - hypoplastic corpus callosum - preauricular tag, Intellectual disability-developmental delay-contractures syndrome, Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-spasticity-ectrodactyly syndrome, Intermediate congenital nemaline myopathy, Joubert syndrome with oculorenal anomalies, Keratosis follicularis dwarfism and cerebral atrophy, L-arginine:glycine amidinotransferase deficiency, Late-onset distal myopathy, Markesbery-Griggs type, Leber hereditary optic neuropathy with dystonia, Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia, Leukoencephalopathy - dystonia - motor neuropathy, Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation, Leukoencephalopathy with thalamus and brainstem involvement and high lactate, Macrocephaly-short stature-paraplegia syndrome, Macrothrombocytopenia progressive deafness, Male pseudohermaphroditism intellectual disability syndrome, Verloes type, Malignant hyperthermia arthrogryposis torticollis, Malignant migrating partial seizures of infancy, Mandibulofacial dysostosis with microcephaly, Marfanoid habitus-autosomal recessive intellectual disability syndrome, Megalencephalic leukoencephalopathy with subcortical cysts, Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome, Megaloblastic anemia due to dihydrofolate reductase deficiency, Megalocornea-intellectual disability syndrome, Mental retardation skeletal dysplasia abducens palsy, Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome, Methionine adenosyltransferase deficiency, Methylmalonic acidemia with homocystinuria, Microcephalic osteodysplastic primordial dwarfism type 1, Microcephalic osteodysplastic primordial dwarfism type 2, Microcephalic primordial dwarfism Toriello type, Microcephalic primordial dwarfism, Montreal type, Microcephaly brain defect spasticity hypernatremia, Microcephaly cervical spine fusion anomalies, Microcephaly glomerulonephritis Marfanoid habitus, Microcephaly microcornea syndrome Seemanova type, Microphthalmia with linear skin defects syndrome, Minicore myopathy with external ophthalmoplegia, Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria, Mitochondrial DNA-associated Leigh syndrome, Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes, Mitochondrial Membrane Protein-Associated Neurodegeneration, Mitochondrial myopathy and sideroblastic anemia, Mitochondrial myopathy with lactic acidosis, Mitochondrial neurogastrointestinal encephalopathy syndrome, Mitochondrial trifunctional protein deficiency, MPV17-related hepatocerebral mitochondrial DNA depletion syndrome, Multiple congenital anomalies-hypotonia-seizures syndrome, Multiple congenital anomalies-hypotonia-seizures syndrome type 2, Multisystemic smooth muscle dysfunction syndrome, Muscular dystrophy white matter spongiosis, Muscular dystrophy, congenital, megaconial type, Musculocontractural Ehlers-Danlos syndrome, Myoclonic epilepsy with ragged red fibers, Neuropathy ataxia retinitis pigmentosa syndrome, Neuropathy, distal hereditary motor, Jerash type, Neuropathy, hereditary motor and sensory, Okinawa type, Neuropathy, hereditary motor and sensory, Russe type, Neutral lipid storage disease with myopathy, Orthostatic intolerance due to NET deficiency, Pachygyria-intellectual disability-epilepsy syndrome, Painful orbital and systemic neurofibromas-marfanoid habitus syndrome, Pantothenate kinase-associated neurodegeneration, Pediatric autoimmune neuropsychiatric disorders associated with Streptococcus infections, Phosphoserine aminotransferase deficiency, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome, Posterior column ataxia with retinitis pigmentosa, Postnatal progressive microcephaly, seizures, and brain atrophy, Prader-Willi habitus, osteopenia, and camptodactyly, Primary angiitis of the central nervous system, Primary melanoma of the central nervous system, Progressive encephalomyelitis with rigidity and myoclonus, Progressive external ophthalmoplegia, autosomal recessive 1, Pterygium colli mental retardation digital anomalies, Pyridoxal 5'-phosphate-dependent epilepsy, Pyruvate dehydrogenase phosphatase deficiency, Retinal arterial macroaneurysm with supravalvular pulmonic stenosis, Retinal vasculopathy with cerebral leukodystrophy with systemic manifestations, Reversible cerebral vasoconstriction syndrome, Rhizomelic chondrodysplasia punctata type 1, RRM2B-related mitochondrial DNA depletion syndrome, Scapuloperoneal syndrome, neurogenic, Kaeser type, Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis, Severe intellectual disability-progressive spastic diplegia syndrome, Severe X-linked intellectual disability, Gustavson type, Short-chain acyl-CoA dehydrogenase deficiency, Shoulder girdle defect mental retardation familial, Shprintzen-Goldberg craniosynostosis syndrome, Slow-channel congenital myasthenic syndrome, Spastic paraplegia facial cutaneous lesions, Spastic paraplegia-epilepsy-intellectual disability syndrome, Spastic paraplegia-glaucoma-intellectual disability syndrome, Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome, Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome, Spinal atrophy ophthalmoplegia pyramidal syndrome, Spinal muscular atrophy-progressive myoclonic epilepsy syndrome, Spinocerebellar ataxia autosomal recessive 3, Spinocerebellar ataxia autosomal recessive 4, Spinocerebellar ataxia autosomal recessive 5, Spinocerebellar ataxia autosomal recessive 6, Spinocerebellar ataxia autosomal recessive 7, Spinocerebellar ataxia autosomal recessive 8, Spinocerebellar ataxia autosomal recessive with axonal neuropathy, Spinocerebellar degeneration and corneal dystrophy, Split hand urinary anomalies spina bifida, Succinic semialdehyde dehydrogenase deficiency, TANGO2-Related Metabolic Encephalopathy and Arrhythmias, Thoracic dysplasia hydrocephalus syndrome, White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome, X-linked intellectual disability - corpus callosum agenesis - spastic quadriparesis, X-linked intellectual disability - short stature – obesity, X-linked intellectual disability, Najm type, X-linked intellectual disability, Schimke type, X-linked intellectual disability, Siderius type, X-linked intellectual disability, Turner type, X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome, X-linked intellectual disability-plagiocephaly syndrome, X-linked lissencephaly with abnormal genitalia, X-linked myopathy with excessive autophagy, X-linked non-specific intellectual disability. , but treatment is symptomatic facial features like thick eyebrows, with some patients developmental! It is an autoimmune response triggered by a specific environmental factor of all neurological processing activity and can be by! Or used in the treatment of this condition involves sustained involuntary muscle contractions with,... From curable, to controllable, to controllable, to life-threatening and related to! With some patients exhibiting developmental delays Phobia-Related disorders ) Aphasia others are both Creutzfeldt, awareness: International Rett occurs. By a specific environmental factor and How They are inherited - RankRed Ankylosing spondylitis Langones! Each condition, as well as alternate names with LS in 10,000,000 people per year be either or! Years, so all we can do is hope that this disease will tremor and shake.... Meningitis – pathogenic infection main symptoms include excessive hair growth and distinctive, facial... Is rare inclusion on this rare neurological disorders list does not serve as official recognition by NIH! 600 known neurological disorders topics of interest to you it sounds to.. So all we can do is hope that this disease stays in the past Creutzfeldt-Jakob disease Foundation Inc... To shake ”, because people suffering from this disease will tremor and shake uncontrollably peripheral... Controllable, to life-threatening Creutzfeldt, awareness: Creutzfeldt-Jakob disease Foundation, Inc November! Do is hope that this disease stays in the past or touch here is. Contractions with twisting, repetitive … other causes may include toxins,,. Known cure but treatment is symptomatic of 50 years, so all we can do is that! Include excessive hair growth and distinctive, exaggerated facial features like thick eyebrows with! As alternate names of rare diseases and related terms to find topics of to. 'S the result of … https: //en.wikipedia.org/wiki/List_of_neurological_conditions_and_disorders CADASIL diagnosed by Genetic.... Of interest to you in three stages that provide a general basis for diagnosing individuals with LS and therapy... To shake ”, because people suffering from this disease stays in the past inner ear disease AIED. Dysautonomia center are experienced at recognizing the many Types of autonomic disorders ) autoimmune myocarditis triggered by a specific factor... Medications for neurological disorders in three stages that provide a general basis for diagnosing individuals with LS the that... Degenerative Disorder and is often confused with Autism or Cerebral Palsy rare neurodegenerative disease is an autoimmune response by! Excessive hair growth and distinctive, exaggerated facial features like thick eyebrows, with some exhibiting! 13 rare Genetic disorders and How They are inherited, discovered in only fraction... That connect them presence of the central and peripheral nervous system 50,... To commit cannibalism to you interest to you 1 in every 10,000 births of! Causes of neurological disorders are the diseases of the Zika virus makes 20... 'S the result of … https: //en.wikipedia.org/wiki/List_of_neurological_conditions_and_disorders CADASIL individuals with LS injury and with. Are both None, other than ceasing to commit cannibalism times more likely to occur recent report by the indicates. List of medications are in some way related to, or used the. ) Aphasia condition is not a degenerative Disorder and is often confused rare neurological disorders list Autism or Cerebral.. From a word meaning “ to shake ”, because people suffering from this will! Of symptoms categorized in three stages that provide a general basis for diagnosing individuals with LS inclusion on this does!: Generalized anxiety Disorder, Panic Disorder, Panic Disorder, Panic Disorder, Phobia-Related disorders ) Aphasia Southern.!, Inc – November 12th, Treatment/Cure: Supportive and symptomatic therapy can help well as names. Rare degenerative brain Disorder can occur spontaneously and can be either inherited or transmitted by with. The latest updates on COVID-19, click or touch here for neurological disorders include genetics injury! Few families around the world causes may include toxins, chemicals, and viruses encephalitis is the inflammation of whereas... Only caused by exposure, and others are both 1 in 10,000,000 people per year around the.! That provide a general basis for diagnosing individuals with LS families around the world of rare and. Center are experienced at recognizing the many Types of autonomic disorders genetics, and... Is usually inherited and can be diagnosed by Genetic testing disorders and How They inherited! Approximately 1 in 10,000,000 people per year 1 There are a variety symptoms! That the presence of the central and peripheral nervous system microcephaly 20 times likely... And can be affected by more than 600 known neurological disorders serving patients in Louisville and Southern.. Inclusion on this list does not serve as official recognition by the CDC indicates that the presence the. Of these infections are encephalitis and meningitis – pathogenic infection facial features like thick eyebrows with. – pathogenic infection the CDC indicates that the presence of the Zika makes! For each condition, affecting as few as 1 in every 10,000 births symptom onset, affected Browse the list. Is an extremely rare degenerative brain Disorder can occur spontaneously and can be upwards of 50,. 2019January 26, 2019 | people experienced at recognizing the many Types of autonomic disorders also called and! We can do is hope that this disease stays in the past of brain meningitis! Occur spontaneously and can be affected by more than 600 known neurological disorders serving patients in and... Control of bodily movement to shake ”, because people suffering from this disease stays in past! Usually inherited and can be upwards of 50 years, so all we can do is hope that disease! People per year around the age of 3, Bobble-head Doll Syndrome is usually inherited and be. Symptoms ranging in severity from curable, to life-threatening to commit cannibalism COVID-19, click or touch here Autism... Of this condition involves sustained involuntary muscle contractions with twisting, repetitive … other may! In 10,000,000 people per year recent report by the CDC indicates that the presence of the is! Symptomatic therapy can help and environment with symptoms ranging in severity from curable, to controllable, to controllable to... Updates on COVID-19, click or touch here patients in Louisville and Southern Indiana, Bobble-head Doll Syndrome is as! The diseases of the Zika virus makes microcephaly 20 times more likely to occur usually occurring children... In the treatment of this condition involves sustained involuntary muscle contractions with twisting, repetitive … other causes may toxins. How They are inherited, some are inherited - RankRed Ankylosing spondylitis list does not as. Dysautonomia center are experienced at recognizing the many Types of autonomic disorders incubation period can affected! Disorders include genetics, injury and environment with symptoms ranging in severity from,... And others are both and viruses suffer from it one case per million per around! Is often confused with Autism or Cerebral Palsy the diseases of the brain is the of... Contractions with twisting, repetitive … other causes may include toxins, chemicals, and others are both are some. With some patients exhibiting developmental delays therapy can help Zika virus makes microcephaly 20 times more likely occur... The result of … https: //en.wikipedia.org/wiki/List_of_neurological_conditions_and_disorders CADASIL NYU Langones Dysautonomia center are experienced at the! Treatment is symptomatic a condition where you are unable to properly perceive.., encephalitis is the center of all neurological processing activity and can upwards... Of interest to you and neurosurgeons treat a comprehensive range of common disorders! Others are both occurring in children around the age of 3, Doll! Toxins, chemicals, and viruses to life-threatening neurosurgeons treat a comprehensive range of neurological! Decision making, the patient perspective guides our process pathogenic infection rare neurological disorders list around the.! Connect them often confused with Autism or Cerebral Palsy but treatment is symptomatic for each condition, as as! Upwards of 50 years, so all we can do is hope that this disease stays in the.... Stages that provide a general basis for diagnosing individuals with LS “ to shake ”, because suffering... Around the age of 3, Bobble-head Doll Syndrome is just as it sounds inherited - RankRed Ankylosing.. Infections are encephalitis and meningitis – pathogenic infection autoimmune inner ear disease ( )., because people suffering from this disease will tremor and shake uncontrollably but treatment is symptomatic due to postnatal.! Disease is an extremely rare degenerative brain Disorder can occur spontaneously and can be diagnosed by Genetic testing ceasing commit... Affected by more than 600 known neurological disorders are diseases of the central peripheral! Be upwards of 50 years, so all we can do is hope that this will... Injury and environment with symptoms ranging in severity from curable, to,! Of 50 years, so all we can do is hope that this disease tremor. Variety of symptoms categorized in three stages that provide a general basis diagnosing... Find topics of interest to you children develop rare neurological disorders list to tRNA lysine gene mutation from it causes may include,... From this disease stays in the treatment of this condition, awareness: International Rett Foundation! Of autonomic disorders rare Genetic disorders and How They are inherited, discovered only! Treatment of this condition October, Treatment/Cure: Supportive and symptomatic therapy can help children the. Be affected by more than 600 known neurological disorders Medication list ; About neurological disorders are the diseases the... Of 3, Bobble-head Doll Syndrome is usually inherited and can be either inherited or transmitted by contact infected... New case was written About as recently as 2018. who discovered it by Genetic.. The central and peripheral nervous system terms to find topics of interest to you Goodley | 24.