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Results 1 - 10 of 12 for Autosomal dominant cerebellar ataxia type I
  1. Degenerative Nerve Diseases (National Library of Medicine)  
    ... serious or life-threatening. It depends on the type. Most of them have no cure. Treatments may help improve symptoms, relieve pain, and increase mobility.
    https://medlineplus.gov/degenerativenervediseases.html - Health Topics
  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. 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
  4. Spinocerebellar ataxia type 6 
    Spinocerebellar ataxia type 6 (SCA6) is a condition characterized by progressive problems with movement. People with this condition initially experience problems ... and symptoms. This phenomenon is called anticipation. SCA6 Type 6 spinocerebellar ataxia Genetic Testing Registry: Spinocerebellar ataxia ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-6 - Genetics
  5. Spinocerebellar ataxia type 36 
    Spinocerebellar ataxia type 36 (SCA36) is a condition characterized by progressive problems with movement that typically begin in mid-adulthood. People ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  6. Autosomal dominant optic atrophy and cataract 
    ... A form of optic atrophy called optic atrophy type 1 accounts for most cases, while autosomal dominant ... parent with the condition. Autosomal dominant optic atrophy type 3 OPA3 OPA3, autosomal dominant Optic atrophy and ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  7. Lissencephaly with cerebellar hypoplasia 
    ... Lissencephaly 2 Lissencephaly 3 Lissencephaly syndrome, Norman-Roberts type Norman-Roberts syndrome Genetic Testing Registry: Lissencephaly type 3 Genetic Testing Registry: Norman-Roberts syndrome Cobblestone ...
    https://medlineplus.gov/.../lissencephaly-with-cerebellar-hypoplasia - Genetics
  8. Charcot-Marie-Tooth disease 
    ... that sometimes leads to deafness.There are several types of Charcot-Marie-Tooth disease, which are differentiated ... effects on nerve cells and patterns of inheritance. Type 1 (CMT1) is characterized by abnormalities in myelin, ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  9. Ataxia-pancytopenia syndrome 
    ... also causes a shortage of one or more types of normal blood cells: red blood cells, white ... A shortage of all three of these cell types is known as pancytopenia. Pancytopenia can result in ...
    https://medlineplus.gov/.../condition/ataxia-pancytopenia-syndrome - Genetics
  10. Spinocerebellar Ataxias Including Machado-Joseph Disease 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 ... Spinocerebellar ...
    https://www.ninds.nih.gov/...taxias-including-machado-joseph-disease - External Health Links
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