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Results 1 - 7 of 7 for Hereditary spastic paraplegia 14
  1. 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.0b013e3181bacf59. Citation ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-15 - Genetics
  2. Spastic paraplegia type 3A 
    ... doi: 10.1093/hmg/ddl054. Epub 2006 Mar 14. Citation on PubMed
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-3a - Genetics
  3. ATL1 gene 
    ... P, Kremensky I, Mitev V, De Jonghe P. Hereditary spastic paraplegia 3A associated with axonal neuropathy. Arch Neurol. 2007 ... Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia. Clin Genet. 2011 Jun;79(6):523-30. ...
    https://medlineplus.gov/genetics/gene/atl1 - Genetics
  4. REEP1 gene 
    ... Arning L, Epplen JT, Stemmler S. Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31). BMC ... Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. Am J Hum Genet. 2006 Aug; ...
    https://medlineplus.gov/genetics/gene/reep1 - Genetics
  5. ALDH18A1 gene 
    ... of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia. Brain. 2015 Aug;138(Pt 8):2191-205. ...
    https://medlineplus.gov/genetics/gene/aldh18a1 - Genetics
  6. TUBB4A-related leukodystrophy 
    ... TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia. Mov Disord. 2015 May;30(6):854-8. ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  7. Patient support and advocacy groups 
    ... Snow Foundation Snyder-Robinson Foundation Soft Bones Spastic Paraplegia Foundation Spinal Muscular Atrophy UK Spondylitis Association of ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -