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Results 1 - 10 of 32 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. Troyer syndrome 
    ... paraplegia involve the legs and the bladder. Complex hereditary spastic paraplegias may include additional signs and symptoms such as intellectual disabilities, problems with coordination and balance (ataxia), and damage to the nerves that connect the ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - 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. Hereditary folate malabsorption 
    ... delays, intellectual disabilities, seizures, and difficulty coordinating movements (ataxia). Abnormal deposits of calcium (calcification) in the brain may also occur. Pregnant people with hereditary folate malabsorption who are receiving treatment for the ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  7. 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
  8. 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
  9. 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
  10. 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
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