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Results 1 - 10 of 33 for Spastic ataxia 2
  1. Autosomal recessive spastic ataxia of Charlevoix-Saguenay 
    ... 1007/s00415-018-8950-4. Epub 2018 Jul 2. Citation on PubMed
    https://medlineplus.gov/...ive-spastic-ataxia-of-charlevoix-saguenay - Genetics
  2. SACS gene 
    ... that is characterized by abnormal tensing of the muscles (spasticity), problems with balance and coordination (cerebellar ataxia), and reduced sensation and weakness in the arms and legs (peripheral neuropathy).Two SACS gene mutations have been found frequently in ...
    https://medlineplus.gov/genetics/gene/sacs - Genetics
  3. Spastic paraplegia type 5A 
    ... EFNS. EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. Eur J Neurol. 2010 Feb;17(2):179-88. doi: 10.1111/j.1468-1331. ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-5a - Genetics
  4. Andermann syndrome 
    ... 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. Citation on ...
    https://medlineplus.gov/genetics/condition/andermann-syndrome - Genetics
  5. Spastic paraplegia type 2 
    ... it can develop later in life. Individuals with spastic paraplegia type 2 ... (ataxia); involuntary movements of the eyes (nystagmus); and involuntary, ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-2 - Genetics
  6. SPG7 gene 
    ... DF. Genomic structure and expression analysis of the spastic paraplegia gene, SPG7. Hum Genet. 1999 Jul-Aug;105(1-2):139-44. doi: 10.1007/s004399900087. Citation on PubMed SPG7 mutations are a common cause of undiagnosed ataxia. Neurology. 2015 May 5;84(18):1911. doi: ...
    https://medlineplus.gov/genetics/gene/spg7 - Genetics
  7. Troyer syndrome 
    ... leg muscles. Hereditary spastic paraplegias are divided into two types: pure and ... and balance (ataxia), and damage to the nerves that connect the ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  8. Transthyretin amyloidosis 
    ... form, amyloidosis occurs in the leptomeninges, which are two thin layers of tissue ... paralysis), seizures, and loss of intellectual function (dementia). ...
    https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis - Genetics
  9. TUBB4A-related leukodystrophy 
    ... with TUBB4A-related leukodystrophy fall in between these two extremes. Affected ... and ataxia without the other movement or learning problems common ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  10. POLR3A gene 
    ... are a frequent cause of sporadic and recessive spastic ataxia. Brain. 2017 Jun 1;140(6):1561-1578. ...
    https://medlineplus.gov/genetics/gene/polr3a - Genetics
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