Unclassified familial myopathy resembling Steinert disease, without myotonia

Telerman Toppet, Nicole; Khoubesserian, P.; Bacq, Michèle; Durdu, Jacques; Lambelin, Dominique; Coërs, Christian

doi:doi/10.1002/mus.880070604

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Unclassified familial myopathy resembling Steinert disease, without myotonia

par Telerman Toppet, Nicole

;Khoubesserian, P.;Bacq, Michèle

;Durdu, Jacques

;Lambelin, Dominique

;Coërs, Christian

Référence Muscle & nerve, 7, 6, page (439-441)
Publication Publié, 1984-08

Article révisé par les pairs

Résumé :

A familial myopathy with predominantly proximal muscle atrophy is described. Although several clinical features such as sternomastoid and brachioradialis muscle involvement suggested Steinert disease, myotonia was not demonstrated by clinical examination or EMG. Histological data were consistent with myotonic dystrophy.

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