| Literature DB >> 19435728 |
Paola Mandich1, Marina Grandis, Alessandra Varese, Alessandro Geroldi, Massimo Acquaviva, Paola Ciotti, Rossella Gulli, Laura Doria-Lamba, Gian Maria Fabrizi, Gaia Giribaldi, Antonio Pizzuti, Angelo Schenone, Emilia Bellone.
Abstract
Mutations in small heat-shock protein 27 and small heat-shock protein 22 genes were found in association with Charcot-Marie-Tooth disease type 2 and distal hereditary motor neuropathy. We searched for mutations in small heat-shock protein 27 gene in an Italian family with peripheral neuropathy and intrafamilial phenotypic variability. A novel heterozygous frame-shift mutation c.476_477delCT was found while point mutations in most genes associated with hereditary neuropathies were ruled out. In the proband, who showed a severe early onset peripheral neuropathy, an independent pathogenetic effect on the peripheral nervous system secondary to the tetanus toxoid injection may be supposed. This is the first truncating nonsense mutation in the small heat-shock protein 27 gene identified so far and the clinical, neurophysiologic, and neuropathological findings are discussed.Entities:
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Year: 2009 PMID: 19435728 DOI: 10.1177/0883073809334387
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987