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Results 1 - 10 of 64 for Progressive truncal ataxia
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  1. PRICKLE1-related progressive myoclonus epilepsy with ataxia 
    ... mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome. Am J Hum Genet. 2008 Nov;83( ...
    https://medlineplus.gov/...rogressive-myoclonus-epilepsy-with-ataxia - Genetics
  2. Cerebral folate transport deficiency 
    ... M, Garcia-Cazorla A, Cormand B, Artuch R. Progressive ataxia and myoclonic epilepsy in a patient with a ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics
  3. Infantile-onset spinocerebellar ataxia 
    Infantile-onset spinocerebellar ataxia (IOSCA) is a progressive disorder that affects the nervous system. Babies with IOSCA develop normally during the first year of life. During early ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  4. Ataxia-telangiectasia 
    ... other body systems. This disorder is characterized by progressive difficulty with coordinating movements (ataxia) beginning in early childhood, usually before age 5. ...
    https://medlineplus.gov/genetics/condition/ataxia-telangiectasia - Genetics
  5. Pelizaeus-Merzbacher disease 
    ... breathing caused by an obstructed airway (stridor), nystagmus, progressive speech difficulties (dysarthria), severe ataxia, hypotonia, and seizures. As the condition worsens, affected ...
    https://medlineplus.gov/.../condition/pelizaeus-merzbacher-disease - Genetics
  6. Spinocerebellar ataxia type 3 
    ... type 3 (SCA3) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination and balance (ataxia). Other early signs and symptoms of SCA3 include ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  7. Spinocerebellar ataxia type 1 
    ... type 1 (SCA1) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination and balance (ataxia). Other signs and symptoms of SCA1 include speech ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  8. Spinocerebellar ataxia type 2 
    ... type 2 (SCA2) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination and balance (ataxia). Other early signs and symptoms of SCA2 include ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  9. Spinocerebellar ataxia type 6 
    ... type 6 (SCA6) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination and balance (ataxia). Other early signs and symptoms of SCA6 include ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-6 - Genetics
  10. Spinocerebellar ataxia type 36 
    Spinocerebellar ataxia type 36 (SCA36) is a condition characterized by progressive problems with movement that typically begin in mid-adulthood. People with this condition initially experience problems with ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
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