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Results 1 - 10 of 23 for Hereditary spastic paraplegia 6
  1. ATL1 gene 
    ... Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia. Clin Genet. 2011 Jun;79(6):523-30. doi: 10.1111/j.1399-0004. ...
    https://medlineplus.gov/genetics/gene/atl1 - Genetics
  2. TUBB4A-related leukodystrophy 
    ... TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia. Mov Disord. 2015 May;30(6):854-8. doi: 10.1002/mds.26196. Epub ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  3. TUBB4A gene 
    ... TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia. Mov Disord. 2015 May;30(6):854-8. doi: 10.1002/mds.26196. Epub ...
    https://medlineplus.gov/genetics/gene/tubb4a - Genetics
  4. Spastic paraplegia type 5A 
    ... CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5. Brain. 2009 Jun;132(Pt 6):1589-600. doi: 10.1093/brain/awp073. Epub ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-5a - Genetics
  5. Spastic paraplegia type 15 
    ... SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. Neurology. 2009 Oct 6;73(14):1111-9. doi: 10.1212/WNL. ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-15 - Genetics
  6. CYP7B1 gene 
    ... CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5. Brain. 2009 Jun;132(Pt 6):1589-600. doi: 10.1093/brain/awp073. Epub ...
    https://medlineplus.gov/genetics/gene/cyp7b1 - Genetics
  7. SPART gene 
    ... Central Lu J, Rashid F, Byrne PC. The hereditary spastic paraplegia protein spartin localises to mitochondria. J Neurochem. 2006 Sep;98(6):1908-19. doi: 10.1111/j.1471-4159. ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
  8. Troyer syndrome 
    ... article on PubMed Central Burgunder JM, Hunziker W. Hereditary spastic paraplegia: clues from a rare disorder for a common problem? IUBMB Life. 2003 Jun;55(6):347-52. doi: 10.1080/1521654032000114311. Citation on ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  9. Spastic paraplegia type 2 
    ... have a normal lifespan. The prevalence of all hereditary spastic paraplegias combined is estimated to be 2 to 6 in 100,000 people worldwide. Spastic paraplegia type 2 likely accounts for only a small ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-2 - Genetics
  10. Spastic paraplegia type 7 
    ... become noticeable in adulthood. The prevalence of all hereditary spastic paraplegias combined is estimated to be 2 to 6 in 100,000 people worldwide. This group of conditions is the most common cause of inherited spasticity. Spastic paraplegia type 7 likely accounts for only a small ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
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