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- J R Yuste, O Beloqui, A De la Peña, R Rodríguez-Rosado, J I Monreal, F Prósper, and J Prieto.
- Departamento de Medicina Interna, Facultad de Medicina, Universidad de Navarra.
- Rev Med Univ Navarra. 1998 Jan 1; 42 (1): 29-33.
AbstractMcArdle's disease (glycogenosis type V) is a metabolic disorder of hydrocarbons, inherited with autosomic recessive pattern. Biochemically is defined by a myophosphorylase deficiency; clinically it is characterized by exercise intolerance, due to the impossibility of providing energetic substrate to the muscle, myalgias and stiffness. We present a case report of a patient with McArdle's disease and we comment the diagnostic procedures and current therapeutic options.
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