[Massive rhabdomyolysis revealing a McArdle disease]. / Rhabdomyolyse massive révélant une maladie de McArdle.
Rev Med Interne
; 28(7): 501-3, 2007 Jul.
Article
em Fr
| MEDLINE
| ID: mdl-17383055
ABSTRACT
INTRODUCTION:
McArdle's disease is an autosomal recessive glycogenosis caused by deficiency of muscle glycogen phosphorylase resulting in glycogen accumulation in the skeletal muscle. Typically, McArdle's disease is characterized by exercise intolerance with muscle cramps and myoglobinuria. CASE REPORT We report a 20-year-old woman with massive rhabdomyolysis and acute renal failure revealing a McArdle's disease.DISCUSSION:
Although muscle impairment is constant in McArdle's disease, massive rhabdomyolysis with severe acute renal failure has been rarely reported as a presenting feature. The mechanisms and therapeutic implications of renal injury are discussed.
Buscar no Google
Base de dados:
MEDLINE
Assunto principal:
Rabdomiólise
/
Doença de Depósito de Glicogênio Tipo V
Idioma:
Fr
Ano de publicação:
2007
Tipo de documento:
Article