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Results 1 - 10 of 10 for Autosomal dominant spastic paraplegia type 9
  1. Spastic paraplegia type 31 
    ... one to 12 per 100,000 individuals. Spastic paraplegia type 31 accounts for 3 to 9 percent of all autosomal dominant hereditary spastic paraplegia cases. Spastic paraplegia type 31 ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-31 - Genetics
  2. Spastic paraplegia type 3A 
    ... a subgroup of hereditary spastic paraplegias known as autosomal dominant hereditary spastic paraplegia, which has an estimated prevalence of 2 to 9 per 100,000 individuals. Spastic paraplegia type 3A accounts for 10 to 15 percent of ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-3a - Genetics
  3. Spastic paraplegia type 8 
    ... Hereditary spastic paraplegia 8 Autosomal dominant spastic paraplegia type 8 ... hereditary spastic paraplegia, on chromosome 8q. Am J Hum Genet. 1999 Feb;64(2):563-9. doi: 10.1086/302258. Citation on PubMed or ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-8 - Genetics
  4. Silver syndrome 
    ... paraplegia 17 Genetic Testing Registry: Hereditary spastic paraplegia Autosomal dominant spastic paraplegia type 17 Hereditary spastic paraplegia National Organization for Rare ...
    https://medlineplus.gov/genetics/condition/silver-syndrome - Genetics
  5. Spastic paraplegia type 7 
    ... symptoms of the condition.In rare cases, spastic paraplegia type 7 is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
  6. Spastic paraplegia type 4 
    ... to the major signs and symptoms of spastic paraplegia type 4. SPAST This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-4 - Genetics
  7. WASHC5 gene 
    ... B, Leppert M, Fink JK. Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q. Am J Hum Genet. 1999 Feb;64(2):563-9. doi: 10.1086/302258. Citation on PubMed or ...
    https://medlineplus.gov/genetics/gene/washc5 - Genetics
  8. REEP1 gene 
    ... Schlang KJ, Arning L, Epplen JT, Stemmler S. Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31). BMC Med Genet. 2008 Jul 21;9:71. doi: 10.1186/1471-2350-9-71. ...
    https://medlineplus.gov/genetics/gene/reep1 - Genetics
  9. OPA3 gene 
    ... G, Bonneau D. OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract. J Med Genet. 2004 Sep;41(9):e110. doi: 10.1136/jmg.2003.016576. No ...
    https://medlineplus.gov/genetics/gene/opa3 - Genetics
  10. Isolated lissencephaly sequence 
    ... or TUBA1A gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered ... cytoskeletal abnormalities in the neuropathology and pathophysiology of type I ... doi: 10.1007/s00401-010-0768-9. Epub 2010 Nov 3. Citation on PubMed or ...
    https://medlineplus.gov/.../isolated-lissencephaly-sequence - Genetics