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Results 1 - 10 of 24 for Acquired ataxia
  1. Ataxias and Cerebellar or Spinocerebellar Degeneration From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Friedreich Ataxia/Related Issues ... Friedreich Ataxia ... Cerebellar Disorders/Start Here ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke
    https://www.ninds.nih.gov/...ebellar-or-spinocerebellar-degeneration - External Health Links
  2. Genetic epilepsy with febrile seizures plus 
    ... development stalls, and some affected children lose already-acquired skills (developmental regression). Many people with Dravet syndrome have difficulty coordinating movements (ataxia) and intellectual disability.Some people with GEFS+ have ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  3. MFSD8 gene 
    ... in early childhood with the loss of previously acquired skills (developmental regression), recurrent seizures (epilepsy), muscle twitches (myoclonus), difficulty coordinating movements (ataxia), speech impairment, and vision loss. Mental functioning and ...
    https://medlineplus.gov/genetics/gene/mfsd8 - Genetics
  4. CLN6 disease 
    ... CLN6 disease initially experience the loss of previously acquired skills (developmental regression). Affected individuals can also develop recurrent seizures (epilepsy), difficulty coordinating movements (ataxia), muscle twitches (myoclonus), impaired speech (dysarthria), and vision ...
    https://medlineplus.gov/genetics/condition/cln6-disease - Genetics
  5. CLN5 disease 
    ... seem like clumsiness, and a loss of previously acquired motor skills (developmental ... movements (ataxia), vision loss, speech problems, and a decline in ...
    https://medlineplus.gov/genetics/condition/cln5-disease - Genetics
  6. CACNA1A gene 
    ... variants is commonly associated with migraines with auras, ataxia, and nystagmus.CACNA1A gene variants that cause sporadic hemiplegic migraine are acquired during a person's lifetime and are not ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  7. Cerebral folate transport deficiency 
    ... around age 2 they begin to lose previously acquired mental and movement abilities ... movements (ataxia) can be severe, and some affected individuals need ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics
  8. SAMD9L gene 
    ... called hepatocellular carcinoma. Unlike the mutations that cause ataxia-pancytopenia syndrome (described above), these genetic changes are somatic, which means they are acquired during a person's lifetime and are present ...
    https://medlineplus.gov/genetics/gene/samd9l - Genetics
  9. Lipid Storage Diseases From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Leukodystrophies/Specifics ... Leukodystrophies ... Tay-Sachs Disease/Related Issues ... Tay-Sachs Disease ... Lipid ...
    https://www.ninds.nih.gov/.../disorders/lipid-storage-diseases - External Health Links
  10. CLN2 disease 
    ... include recurrent seizures (epilepsy) and difficulty coordinating movements ... (developmental regression), intellectual disability that gradually gets ...
    https://medlineplus.gov/genetics/condition/cln2-disease - Genetics
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