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Autosomal dominant spastic paraplegia type 9
- ... 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 ...
- ... 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 ...
- ... symptoms of spastic paraplegia type 8. WASHC5 Spastic paraplegia type 8 is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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. ...
- ... Organization for Rare Disorders (NORD) ClinicalTrials.gov SPASTIC PARAPLEGIA ... Epub 2008 Jul 9. Citation on PubMed Rowland LP, Bird TD. Silver ...
- ... 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 ...
- ... 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 ...
