{"title":"复发性横纹肌溶解和脊柱侧凸的常染色体显性家族史:导致代谢性肌病诊断的临床特征","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":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"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\":null,\"pages\":null},\"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}","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}
Recurrent rhabdomyolysis and an autosomal dominant family history of scoliosis: clinical features leading to a diagnosis of metabolic myopathy
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.