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Results 1 - 10 of 33 for Spinocerebellar ataxia
  1. 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 ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  2. Spinocerebellar ataxia type 1 
    Spinocerebellar ataxia type 1 (SCA1) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  3. Spinocerebellar ataxia type 6 
    Spinocerebellar ataxia type 6 (SCA6) is a condition characterized by progressive problems with movement. People with this condition ... This phenomenon is called anticipation. SCA6 Type 6 spinocerebellar ataxia Genetic Testing Registry: Spinocerebellar ataxia type 6 Spinocerebellar ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-6 - Genetics
  4. Spinocerebellar ataxia type 3 
    Spinocerebellar ataxia type 3 (SCA3) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  5. Spinocerebellar ataxia type 2 
    Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. People with this condition ... be one of the most common types of spinocerebellar ataxia; however, all types of spinocerebellar ataxia are relatively ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  6. 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 ... hypacusis, and athetosis Genetic Testing Registry: Infantile onset ... Infantile-onset spinocerebellar ataxia Mitochondrial DNA depletion syndrome ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  7. Ataxia with oculomotor apraxia 
    ... with ocular motor apraxia and hypoalbuminemia SCAN2 SCAR1 Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia, recessive, non-Friedreich type 1 Genetic Testing Registry: ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  8. Boucher-Neuhäuser syndrome 
    ... with hypogonadism and choroidal dystrophy syndrome Chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism Spinocerebellar ataxia, hypogonadotropic hypogonadism, and ...
    https://medlineplus.gov/.../condition/boucher-neuhauser-syndrome - Genetics
  9. X-linked sideroblastic anemia and ataxia 
    ... X-linked sideroblastic anaemia with ataxia X-linked spinocerebellar ataxia-6 with or without sideroblastic anemia XLSA/A ... anemia with ataxia X-linked sideroblastic anemia and spinocerebellar ataxia National Organization for Rare Disorders (NORD) SPINOCEREBELLAR ATAXIA, ...
    https://medlineplus.gov/.../x-linked-sideroblastic-anemia-and-ataxia - Genetics
  10. Myoclonic epilepsy myopathy sensory ataxia 
    ... adulthood. This condition had previously been known as spinocerebellar ataxia with epilepsy (SCAE).The first symptom of MEMSA ... signs and symptoms of the condition. MEMSA SCAE Spinocerebellar ataxia with epilepsy Genetic Testing Registry: Spinocerebellar ataxia with ...
    https://medlineplus.gov/...yoclonic-epilepsy-myopathy-sensory-ataxia - Genetics
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