| Literature DB >> 21107874 |
Olimpia Musumeci1, Maria Teresa Bassi, Anna Mazzeo, Marina Grandis, Claudia Crimella, Andrea Martinuzzi, Antonio Toscano.
Abstract
Hereditary spastic paraplegias (HSPs) include a group of neurodegenerative diseases, and so far 46 SPG loci have been mapped and 17 genes isolated. Among the autosomal dominant HSPs (AD-HSPs), SPG10 is a rare form due to mutations in KIF5A gene (locus 12q13.3). We describe the clinical, neurophysiological, morphological and genetic study of an Italian family with AD-HSP. The proband presented with an adult onset spastic paraparesis and diffuse paresthesias where neurophysiological and nerve biopsy morphological studies revealed an axonal neuropathy. Molecular genetic analysis identified a new missense mutation (c.608C>G) of KIF5A gene resulting in a serine to cysteine substitution, S203C, located in a highly conserved domain of the protein. This pedigree confirms the occurrence of an axonal peripheral neuropathy in SPG10.Entities:
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Year: 2010 PMID: 21107874 DOI: 10.1007/s10072-010-0445-8
Source DB: PubMed Journal: Neurol Sci ISSN: 1590-1874 Impact factor: 3.307