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Results 1 - 10 of 12 for Acquired ataxia
  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. Prion disease 
    ... prion disease are classified as either sporadic or acquired. People with sporadic prion disease have no family ... insomnia (sFI), and variably protease-sensitive prionopathy (VPSPr).Acquired prion disease results from exposure to PrPSc from ...
    https://medlineplus.gov/genetics/condition/prion-disease - Genetics
  10. Tay-Sachs disease 
    ... normal developmental milestones and begin to lose previously acquired skills such as turning over, sitting, and crawling. ... disease include muscle weakness, loss of muscle coordination (ataxia), speech problems, and psychiatric symptoms. These signs and ...
    https://medlineplus.gov/genetics/condition/tay-sachs-disease - Genetics
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