Glycogen storage disease due to muscle phosphoglycerate mutase deficiency (Q84788): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A deficiência de fosfoglicerato mutase muscular é uma miopatia metabólica caracterizada por cãimbras induzidas por exercício, mioglobinúria e presença de agregados tubulares na biópsia muscular. | |||
| description / en | description / en | ||
Muscle phosphoglycerate mutase deficiency (PGAMD) is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy. | |||
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. |
