Glycogen storage disease due to muscle phosphoglycerate mutase deficiency (Q84788): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
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 |
|---|---|---|---|
| default for all languages | ID_357512951 |
||
| 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. |
Statements
CID11:ID_357512951
0 references
dki-india-ID_357512951
0 references
Concluído
0 references
