Moore D M, Nadarajan P, Hawksworth R, Lane S J, Graham I M
AMNCH, Tallaght, Dublin 24.
Ir Med J. 2011 May;104(5):151.
This case report outlines the diagnoses of a rare myophosphorylase deficiency (McArdle Syndrome) in a unique way. A set of characteristic values from a Cardiopulmonary Exercise Test (CPET) combined with a typical patient history pointed to a failure of the glycolytic pathway in the skeletal muscle. McArdle Syndrome was confirmed with a skeletal muscle biopsy. There is no evidence of such a diagnostic method in the literature.