McArdle’s disease: A case of exercise intolerance and myopathy
McArdle disease is a hereditary glycogen storage disorder caused by a deficiency in the enzyme myophosphorylase, leading to impaired glycogen breakdown in skeletal muscles. Muscle cramping, exercise intolerance, and the possibility of rhabdomyolysis are the outcomes of this. A 25-year-old male with...
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| Principais autores: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Medknow Publications
2025-04-01
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| Colecção: | Journal of Dr. NTR University of Health Sciences |
| Assuntos: | |
| Acesso em linha: | https://journals.lww.com/10.4103/jdrntruhs.jdrntruhs_110_24 |
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