{"title":"Recurrent rhabdomyolysis and an autosomal dominant family history of scoliosis: clinical features leading to a diagnosis of metabolic myopathy","authors":"S. Wright, S. Brady","doi":"10.17161/rrnmf.v3i3.16318","DOIUrl":null,"url":null,"abstract":"Exertional rhabdomyolysis is typically associated with metabolic or mitochondrial myopathies; however, there are important causes such as muscular dystrophies. Herein we describe a case of recurrent exertional rhabdomyolysis in which the diagnosis of RYR1 associated disease was made on clinical presentation avoiding the need for extensive or invasive investigation.","PeriodicalId":309700,"journal":{"name":"RRNMF Neuromuscular Journal","volume":"47 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RRNMF Neuromuscular Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17161/rrnmf.v3i3.16318","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Exertional rhabdomyolysis is typically associated with metabolic or mitochondrial myopathies; however, there are important causes such as muscular dystrophies. Herein we describe a case of recurrent exertional rhabdomyolysis in which the diagnosis of RYR1 associated disease was made on clinical presentation avoiding the need for extensive or invasive investigation.