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Results 1 - 10 of 14 for Autosomal dominant cerebellar ataxia
  1. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCADN) is a nervous system disorder with signs and symptoms that usually begin in mid-adulthood ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  2. DNMT1 gene 
    ... in people with a nervous system disorder called autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCADN). Features of this disorder ... Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy. Clin Epigenetics. 2016 Sep 5; ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  3. Degenerative Nerve Diseases (National Library of Medicine)  
    Degenerative nerve diseases affect many of your body's activities, such as balance, movement, talking, breathing, and heart function. Many of these diseases are genetic. ...
    https://medlineplus.gov/degenerativenervediseases.html - Health Topics
  4. CACNA1A gene 
    ... Dobyns WB, Subramony SH, Zoghbi HY, Lee CC. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  5. Autosomal dominant optic atrophy and cataract 
    ... shades of blue and green.Some people with autosomal dominant optic atrophy and ... (cerebellar ataxia), an unsteady style of walking (gait), prickling or ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  6. Spinocerebellar ataxia type 36 
    ... affected by expansion of the gene, leading to cerebellar atrophy. Deterioration in this part of the brain leads to ataxia and the other signs and symptoms of SCA36. NOP56 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  7. Gillespie syndrome 
    ... no history of the disorder in their family. Autosomal dominant cases of Gillespie syndrome are ... ataxia, and mental retardation Aniridia-cerebellar ataxia-intellectual disability ...
    https://medlineplus.gov/genetics/condition/gillespie-syndrome - Genetics
  8. Charcot-Marie-Tooth disease 
    ... MOTOR AND SENSORY, WITH EXCESSIVE MYELIN FOLDING COMPLEX, AUTOSOMAL RECESSIVE ... DOMINANT, 1; CMTX1 NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  9. Ataxias and Cerebellar or Spinocerebellar Degeneration From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Friedreich Ataxia/Related Issues ... Friedreich Ataxia ... Cerebellar Disorders/Start Here ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke
    https://www.ninds.nih.gov/...ebellar-or-spinocerebellar-degeneration - External Health Links
  10. Ataxia-pancytopenia syndrome 
    ... leukemia. SAMD9L ... B, Baranko PV, Potter NU. Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous ...
    https://medlineplus.gov/.../condition/ataxia-pancytopenia-syndrome - Genetics
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