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Results 1 - 10 of 51 for Progressive cerebellar ataxia
  1. Learning about Fragile X Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Fragile X syndrome is an inherited intellectual disability caused by a mutation in the FMR1 gene. ... Fragile X Syndrome/Start Here ... Fragile X Syndrome ... National ...
    https://www.genome.gov/Genetic-Disorders/Fragile-X-Syndrome - External Health Links
  2. 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
  3. 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
  4. Cerebellar Degeneration From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Specifics ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Cerebellar ...
    https://www.ninds.nih.gov/.../disorders/cerebellar-degeneration - External Health Links
  5. 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
  6. 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
  7. 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
  8. About Ataxia-Telangiectasia (Ataxia-Telangiectasia Children's Project)  
    Ataxia Telangiectasia/Learn More ... Ataxia Telangiectasia ... Ataxia-Telangiectasia Children's Project
    https://atcp.org/learn-about-a-t - External Health Links
  9. 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
  10. 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
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