Open AccessRecurrent rhabdomyolysis and an autosomal dominant family history of scoliosis: clinical features leading to a diagnosis of metabolic myopathy
Author(s) -
Sarah Wright,
Stefen Brady
Publication year - 2022
Publication title -
rrnmf neuromuscular journal
Language(s) - English
Resource type - Journals
ISSN - 2692-3092
DOI - 10.17161/rrnmf.v3i3.16318
Subject(s) - rhabdomyolysis , myopathy , scoliosis , family history , medicine , congenital myopathy , pediatrics , surgery , muscle biopsy , biopsy