| Literature DB >> 6934069 |
R C Sengers, A M Stadhouders, H H Jaspar, K J Lamers, J M Trijbels, S L Notermans.
Abstract
Myophosphorylase deficiency (McArdle's syndrome) is an uncommon condition characterized by exercise intolerance, muscle cramps and myoglobinuria. The present report describes the clinical, histochemical, electronmicroscopic and biochemical findings in a 12-year-old boy with myophosphorylase deficiency. The diagnosis should have been suspected when the boy was 6 years old. Most index cases have not been diagnosed until adult life, but this syndrome has to be considered in the differential diagnosis of exercise intolerance in childhood.Entities:
Mesh:
Year: 1980 PMID: 6934069 DOI: 10.1007/bf01846039
Source DB: PubMed Journal: Eur J Pediatr ISSN: 0340-6199 Impact factor: 3.183