McArdle disease is the most common metabolic myopathy with autosomal recessive inheritance due to mutations in the gene PYGM encoding myophosphorylase. In this report, we describe the first case of a patient affected by MS and McArdle disease
A rare case of multiple sclerosis and McArdle disease
ZOCCOLELLA, STEFANO;DIRENZO, VITA;TROIANO, Maria
2015-01-01
Abstract
McArdle disease is the most common metabolic myopathy with autosomal recessive inheritance due to mutations in the gene PYGM encoding myophosphorylase. In this report, we describe the first case of a patient affected by MS and McArdle diseaseFile in questo prodotto:
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