Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 33 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. Autosomal recessive cerebellar ataxia type 1 
    Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a condition characterized by progressive problems with movement due to a loss (atrophy) of nerve cells in the part of the brain that ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  3. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    ... 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/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  4. 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
  5. Autosomal dominant optic atrophy and cataract 
    ... can lead to problems with balance and coordination (cerebellar ataxia), an unsteady style of walking (gait), prickling or tingling sensations (paresthesias) in the arms and legs, progressive muscle stiffness (spasticity), or rhythmic shaking (tremors). In ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  6. Spinocerebellar ataxia type 6 
    ... the Ca(V)2.1 calcium channel in cerebellar ataxias. F1000 Biol Rep. 2010 Jan 18;2:4. doi: 10.3410/B2-4. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-6 - Genetics
  7. PRICKLE1-related progressive myoclonus epilepsy with ataxia 
    ... A, Leshinsky E, Berkovic SF. An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures. Neurology. 2005 Jan 11;64(1):142-4. doi: 10.1212/01.WNL.0000148600.60470.E6. Citation on PubMed
    https://medlineplus.gov/...rogressive-myoclonus-epilepsy-with-ataxia - Genetics
  8. Spinocerebellar ataxia type 3 
    ... magnetic resonance imaging features of the brainstem and cerebellum and clinical features of spinocerebellar ataxia 3/Machado-Joseph disease. Neurol India. 2009 Sep-Oct;57(5):578-83. doi: 10.4103/0028-3886.57803. Citation on PubMed
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  9. 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
  10. 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
previous · 1 · 2 · 3 · 4 · next