| Literature DB >> 12210373 |
Dianna Quan1, Jeffrey A Cohen.
Abstract
Hereditary amyloidosis with early and prominent peripheral nerve involvement is often designated familial amyloid polyneuropathy (FAP). The abnormality usually lies in the transthyretin (TTR) gene. We describe a patient with a tyr77 TTR gene mutation who presented with sensorimotor polyneuropathy but no other systemic symptoms of amyloidosis. This is one of a few documented cases of the tyr77 mutation in North America. The clinical and electrophysiologic features of this unusual cause of sensorimotor polyneuropathy are discussed. Copyright 2002 Wiley Periodicals, Inc.Entities:
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Year: 2002 PMID: 12210373 DOI: 10.1002/mus.10208
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217