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Results 1 - 10 of 14 for Hereditary spastic paraplegia 16
  1. SPG11 gene 
    ... mutations are common in familial cases of complicated hereditary spastic paraplegia. Neurology. 2008 Apr 15;70(16 Pt 2):1384-9. doi: 10.1212/01.wnl.0000294327.66106.3d. Epub 2008 Mar 12. Citation on PubMed or Free article on ... spastic paraplegia because of Spatacsin mutations (SPG11). Eur J Neurol. ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  2. Spastic paraplegia type 11 
    ... mutations are common in familial cases of complicated hereditary spastic paraplegia. Neurology. 2008 Apr 15;70(16 Pt 2):1384-9. doi: 10.1212/01.wnl.0000294327.66106.3d. Epub 2008 Mar 12. Citation on PubMed or Free article on ... spastic paraplegia because of Spatacsin mutations (SPG11). Eur J Neurol. ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-11 - Genetics
  3. Troyer syndrome 
    ... Natl Acad Sci U S A. 2024 Jan 16;121(3):e2314093121. doi: 10.1073/pnas.2314093121. Epub 2024 Jan 8. Citation on PubMed
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  4. REEP1 gene 
    ... j.brainres.2013.12.008. Epub 2013 Dec 16. Citation on PubMed or Free article on PubMed Central Schlang KJ, Arning L, Epplen JT, Stemmler S. Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31). BMC ...
    https://medlineplus.gov/genetics/gene/reep1 - Genetics
  5. Spastic paraplegia type 3A 
    ... 1468-1331.2012.03665.x. Epub 2012 Feb 16. Citation on PubMed Namekawa M, Ribai P, Nelson I, Forlani S, Fellmann F, Goizet C, Depienne C, Stevanin G, Ruberg M, Durr A, Brice A. SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years. Neurology. 2006 ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-3a - Genetics
  6. Spastic paraplegia type 2 
    ... inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic ... themes emerge in the hereditary spastic paraplegias. J Med Genet. 2003 Feb;40( ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-2 - Genetics
  7. ATL1 gene 
    ... 1468-1331.2012.03665.x. Epub 2012 Feb 16. Citation on PubMed ... and REEP1 in hereditary spastic paraplegia. Clin Genet. 2011 Jun;79(6):523-30. ...
    https://medlineplus.gov/genetics/gene/atl1 - Genetics
  8. Spastic paraplegia type 7 
    ... each cell is sufficient to cause the disorder. Hereditary spastic paraplegia, paraplegin type Spastic paraplegia 7 Genetic Testing Registry: Hereditary spastic paraplegia Genetic Testing Registry: Hereditary spastic paraplegia 7 Hereditary ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
  9. Silver syndrome 
    ... movement and sensations. Silver syndrome is a complex hereditary spastic paraplegia.The first sign of Silver syndrome is usually ... of hands and feet SPG17 Genetic Testing Registry: Hereditary spastic paraplegia 17 Genetic Testing Registry: Hereditary spastic paraplegia Autosomal ...
    https://medlineplus.gov/genetics/condition/silver-syndrome - Genetics
  10. SPART gene 
    ... Troyer syndrome. Troyer syndrome is a type of hereditary spastic paraplegia (also called hereditary spastic paraparesis), a group of ... PubMed Lu J, Rashid F, Byrne PC. The hereditary spastic paraplegia protein spartin localises to mitochondria. J Neurochem. 2006 ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
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