Glycogen storage disease due to muscle phosphoglycerate mutase deficiency (Q84788): Difference between revisions
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Revision as of 10:08, 15 August 2026
Muscle phosphoglycerate mutase deficiency (PGAMD) is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy.
| Language | Label | Description | Also known as |
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| default for all languages | ID_357512951 |
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| English | Glycogen storage disease due to muscle phosphoglycerate mutase deficiency |
Muscle phosphoglycerate mutase deficiency (PGAMD) is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy. |
