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Results 1 - 10 of 12 for Progressive cerebellar ataxia
  1. COQ8B gene 
    ... Smeets H. Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy. Mitochondrion. 2010 Aug;10(5):510- ...
    https://medlineplus.gov/genetics/gene/coq8b - Genetics
  2. DNMT1 gene 
    ... P, Smith AM, Warman Chardon J. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) associated with progressive cognitive and behavioral deterioration. Neuropsychology. 2017 Mar;31( ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  3. CACNA1A gene 
    ... JC, Baloh RW. CACNA1A mutations causing episodic and progressive ataxia alter ... cerebellar ataxia (SCA6) associated with small polyglutamine expansions in ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  4. GRN gene 
    ... the brain leads to the development of epilepsy, cerebellar ataxia, and other signs ... condition is a progressive brain disorder that can affect behavior, language, and ...
    https://medlineplus.gov/genetics/gene/grn - Genetics
  5. PNKP gene 
    ... van de Spek P, Kremer A, Mancini GM. Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP ...
    https://medlineplus.gov/genetics/gene/pnkp - Genetics
  6. 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
  7. 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
  8. 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
  9. 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
  10. 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
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