[Eulenburg's paramyotonia congenita].

doi:10.1016/s0035-3787(07)74181-4

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Article

[Eulenburg's paramyotonia congenita].

Revue neurologique - 1 Nov 2007

Sallansonnet-Froment M, Bounolleau P, De Greslan T, Ricard D, Taillia H, Renard J-L

Abstract excerpt

INTRODUCTION: Paramyotonia congenita is an autosomal dominant sodium channelopathy, caused by mutations in gene coding for muscle voltage-gated sodium channel alpha subunit. CASE REPORT: We report the case of a 38-year-old man who described since childhood muscle stiffness with attacks ok weakness induced by two provocative stimuli: cold exposure and exercise. It primarily concerned eyelids and hands,...

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Identifiers

PMID: 18033047
DOI: 10.1016/s0035-3787(07)74181-4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.