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Results 1 - 10 of 30 for Hereditary ataxia
  1. Andermann syndrome 
    ... Dupre N, Bouchard JP, Brais B, Rouleau GA. Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian population. Can J Neurol Sci. 2006 May;33(2):149-57. doi: 10.1017/s031716710000490x. ... S, Rouleau GA. Hereditary motor and sensory neuropathy with agenesis of the ...
    https://medlineplus.gov/genetics/condition/andermann-syndrome - Genetics
  2. X-linked sideroblastic anemia and ataxia 
    ... Pagon RA, Bird TD, Detter JC, Pierce I. Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder. J Med Genet. ...
    https://medlineplus.gov/.../x-linked-sideroblastic-anemia-and-ataxia - Genetics
  3. Hereditary folate malabsorption 
    ... may develop intellectual disability and difficulty coordinating movements (ataxia). The prevalence of hereditary folate malabsorption is unknown. Approximately 15 affected families ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  4. Charcot-Marie-Tooth disease 
    ... X-LINKED RECESSIVE, 4, WITH OR WITHOUT CEREBELLAR ATAXIA; CMTX4 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5; CMTX5 ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  5. Spastic paraplegia type 7 
    ... either the pure or complex form.Like all hereditary spastic paraplegias, spastic paraplegia type 7 involves spasticity of the leg muscles and some muscle weakness. People with this form of spastic paraplegia can also have ataxia; a pattern of movement abnormalities known as parkinsonism; ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
  6. DNMT1 gene 
    ... in people with another nervous system disorder called hereditary sensory and ... do not have the ataxia or narcolepsy that occurs in ADCADN, and the ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  7. Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report?: ... 
    ... also called G6PD deficiency Hereditary hemochromatosis Transthyretin ... recessive spastic ataxia of Charlevoix-Saguenay , also called ARSACS Andermann syndrome , ...
    https://medlineplus.gov/.../dtcgenetictesting/dtcghrpages - Genetics
  8. Brain-lung-thyroid syndrome 
    ... thyroid syndrome has brain-related movement abnormalities. Benign hereditary ... muscle twitches (myoclonus), and involuntary muscle contractions that ...
    https://medlineplus.gov/.../condition/brain-lung-thyroid-syndrome - Genetics
  9. Marinesco-Sjögren syndrome 
    ... destroys cells in many different tissues, leading to ataxia, myopathy, and the other features of Marinesco-Sjögren ... MSS ...
    https://medlineplus.gov/.../condition/marinesco-sjogren-syndrome - Genetics
  10. KCNA1 gene 
    ... ER, Smith EA, Kramer P, Litt M. Episodic ataxia/myokymia syndrome is associated ... (KCNA1) mutation in hereditary myokymia. Neurogenetics. 2007 Apr;8(2):131-5. ...
    https://medlineplus.gov/genetics/gene/kcna1 - Genetics
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