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Glycogen storage disease II
rareGlycogen storage disease due to acid maltase deficiency (AMD) is an autosomal recessive trait leading to metabolic myopathy that affects cardiac and respiratory muscles in addition to skeletal muscle and other tissues. AMD represents a wide spectrum of clinical presentations caused by an accumulation of glycogen in lysosomes: Glycogen storage disease due to acid maltase deficiency, infantile onset, non-classic infantile onset and adult onset. Early onset forms are more severe and often fatal.
- Identifiers
- MONDO:0009290 Orphanet:365
- Causal genes
- GAA
- Part of
- Disorder of glycogen metabolismFamilial restrictive cardiomyopathyLysosomal glycogen storage disease
- Also known as
- acid maltase deficiency · acid maltase deficiency disease · Aglucosidase alfa · Alpha-1,4-glucosidase acid deficiency · deficiency of alpha-glucosidase
Subtypes
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