[Recent advances of study on hereditary spastic paraplegia type 11]
- PMID: 19953491
- DOI: 10.3760/cma.j.issn.1003-9406.2009.06.013
[Recent advances of study on hereditary spastic paraplegia type 11]
Abstract
The hereditary spastic paraplegias (HSPs) are a large group of inherited, heterogeneous neurological disorders. All modes of inheritance have been reported. SPG11-associated HSP is supposed to be the most common type of complicated autosomal recessive HSP (ARHSP), especially for patients with thin corpus callosum and intelligence disorder. Here we review the mapping and cloning of the SPG11 gene, the clinical features and the supposed pathogenic mechanisms of SPG11 gene abnormalities.
Similar articles
-
Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum.Neuropediatrics. 2006 Apr;37(2):59-66. doi: 10.1055/s-2006-923982. Neuropediatrics. 2006. PMID: 16773502
-
Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset.Neuropediatrics. 2005 Aug;36(4):274-8. doi: 10.1055/s-2005-872809. Neuropediatrics. 2005. PMID: 16138254
-
A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum.J Neurol Sci. 2011 Jun 15;305(1-2):67-70. doi: 10.1016/j.jns.2011.03.011. Epub 2011 Mar 25. J Neurol Sci. 2011. PMID: 21440262
-
[AAA ATPases and hereditary spastic paraplegia].Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Jun;26(3):298-301. doi: 10.3760/cma.j.issn.1003-9406.2009.03.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19504443 Review. Chinese.
-
Genetics of hereditary spastic paraplegias.Semin Neurol. 2011 Nov;31(5):484-93. doi: 10.1055/s-0031-1299787. Epub 2012 Jan 21. Semin Neurol. 2011. PMID: 22266886 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources