| Literature DB >> 15468048 |
Jan Minde1, Göran Toolanen, Thomas Andersson, Inger Nennesmo, Ingela Nilsson Remahl, Olle Svensson, Göran Solders.
Abstract
We have studied a large Swedish family with a mutation in the nerve growth factor beta (NGFB) gene causing insensitivity to deep pain without anhidrosis (hereditary sensory and autonomic neuropathy, type V; HSAN V). Painfree joint destruction and fractures were common. Peripheral nerve conduction was normal, but temperature thresholds were increased. Sural nerve biopsies showed a moderate loss of A delta fibers and a severe reduction of C fibers. The three most severely affected cases were all born to consanguineous parents, and were homozygotes for the causal genetic mutation. Treatment of these patients is discussed.Entities:
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Year: 2004 PMID: 15468048 DOI: 10.1002/mus.20172
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217