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Results 21 - 30 of 33 for Progressive cerebellar ataxia
  1. ATXN2 gene 
    ... Lastres-Becker I, Rub U, Auburger G. Spinocerebellar ataxia 2 (SCA2). Cerebellum. 2008;7(2):115-24. doi: 10.1007/ ...
    https://medlineplus.gov/genetics/gene/atxn2 - Genetics
  2. FMR1 gene 
    ... tremor/ataxia syndrome (FXTAS). FXTAS is characterized by progressive problems with movement (ataxia), tremor, memory loss, reduced sensation in the lower ...
    https://medlineplus.gov/genetics/gene/fmr1 - Genetics
  3. Spinocerebellar ataxia type 36 
    ... SCA36.Brain imaging of people with SCA36 shows progressive atrophy of various parts of the brain, particularly within the cerebellum, which is the area of the brain involved ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  4. ATM gene 
    ... cause ataxia-telangiectasia. This disorder is characterized by progressive difficulty with coordinating movements (ataxia) beginning in early childhood. People with this disorder ...
    https://medlineplus.gov/genetics/gene/atm - Genetics
  5. 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
  6. NOP56 gene 
    ... the gene, leading to cell death in the cerebellum. Deterioration in this part of the brain leads to ataxia and the other signs and symptoms of SCA36. ...
    https://medlineplus.gov/genetics/gene/nop56 - Genetics
  7. CLN10 disease 
    ... and often develop problems with balance and coordination (ataxia), loss of speech, a progressive loss in intellectual functioning (cognitive decline), and vision ...
    https://medlineplus.gov/genetics/condition/cln10-disease - Genetics
  8. Pol III-related leukodystrophy 
    ... and symptoms of the condition. 4H syndrome ADDH Ataxia, delayed dentition, and hypomyelination Dentoleukoencephalopathy HCAHC HLD7 HLD8 Hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum Hypomyelination, ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  9. TPP1 gene 
    ... to-side (oculomotor apraxia). People with SCAR7 have progressive loss of cells (atrophy) of various parts of the brain, particularly within the cerebellum, which is the area of the brain involved ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  10. ATXN3 gene 
    ... the first stage of protein production (transcription). Spinocerebellar ataxia type 3 (SCA3) is a condition characterized by progressive problems with movement. SCA3 results from a mutation ...
    https://medlineplus.gov/genetics/gene/atxn3 - Genetics
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