Glycogen storage disease due to muscle glycogen phosphorylase deficiency (Q84790): Difference between revisions
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Deficiência de miofosforilase (Doença de McArdle) ou doença do depósito de glicogênio do tipo 5 é uma forma grave de doença de depósito de glicogênio caracterizada por intolerância ao exercício com mialgia, cãimbra, fadiga e fraqueza muscular. | |||
| description / en | description / en | ||
Myophosphorylase deficiency (McArdle's disease), or glycogen storage disease type 5 (GSD5), is a severe form of glycogen storage disease characterised by exercise intolerance with myalgia, cramps, fatigue, and muscle weakness. | |||
Revision as of 10:08, 15 August 2026
Myophosphorylase deficiency (McArdle's disease), or glycogen storage disease type 5 (GSD5), is a severe form of glycogen storage disease characterised by exercise intolerance with myalgia, cramps, fatigue, and muscle weakness.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1934070304 |
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| English | Glycogen storage disease due to muscle glycogen phosphorylase deficiency |
Myophosphorylase deficiency (McArdle's disease), or glycogen storage disease type 5 (GSD5), is a severe form of glycogen storage disease characterised by exercise intolerance with myalgia, cramps, fatigue, and muscle weakness. |
