Urinary glycosaminoglycan excretion in healthy subjects and in patients with mucopolysaccharidoses.

Abstract

BACKGROUND The mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders caused by deficiency of enzymes catalyzing the stepwise degradation of glycosaminoglycans (GAGs), and are transmitted in an autosomal recessive manner, except for Hunter syndrome. METHODS The levels of GAGs in 150 healthy subjects and 33 patients with MPS were determined… (More)

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