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[McArdle's disease in adults: clinical and genetic study].

作者信息

Olmos J M, Zarrabeitia M T, Valero M C, Figols J, Matorras P, Riancho J A

机构信息

Departamento de Medicina Interna, Hospital Marqués de Valdecilla, Santander.

出版信息

Med Clin (Barc). 1997 Nov 29;109(19):753-5.

PMID:9470186
Abstract

McArdle's disease is a rare metabolic myopathy resulting from an absence of functional muscle glycogen phosphorylase that is inherited as an autosomal recessive condition. Recent molecular genetic studies have identified more than ten different mutations in patients with McArdle's disease, although a nonsense point mutation at codon 49 in exon 1 (R49X) accounts for approximately 85% of mutant alleles in American and British patients. We describe clinical, biochemical and genetic characteristics of five adults patients with McArdle's disease studied at our hospital during the last 10 years.

摘要

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