Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2951
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dc.contributor.authorSingh, G.en
dc.contributor.authorMcGill, J.en
dc.contributor.authorSabet, A.en
dc.contributor.authorDer, Y. S.en
dc.date.accessioned2022-11-07T23:36:59Z-
dc.date.available2022-11-07T23:36:59Z-
dc.date.issued2020en
dc.identifier.citation50 , 2020, p. 19en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/2951-
dc.description.abstractBackground: Metabolic myopathy, an uncommon cause of rhabdomyolysis, is a rare condition which develops when there is a mismatch between energy supply and demand in muscle cells due to an underlying defect in glucose, glycogen, lipid or nucleoside metabolism1. The heterogenous group of genetic disorders that result from defects in fatty acid oxidation includes very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency. Individuals with an adult onset defect in fatty acid oxidation typically present with exercise or illness induced rhabdomyolysis but may present with weakness and fatigue2. The general approach to these patients encompasses prolonged fasting avoidance, a high complex carbohydrate, low fat diet with medium chain triglyceride (MCTs) and, if needed, essential fatty acid supplementation3. Case Report: A 42-year-old female presented with one-day history of severe myalgia and dark urine after prolonged hiking. This was on a background history of myalgias post physical exertion since childhood and one past episode of atraumatic rhabdomyolysis after extreme dieting and clomiphene use. Family history revealed a brother who reported a similar muscle disorder. On presentation, laboratory evaluation showed marked elevation of plasma crea-tine kinase (85,400). Subsequent acylcarnitine profile by tandem mass spec-trometry demonstrated an abnormal pattern consistent with VLCAD deficiency. The patient was advised to have regular glucose intake frequently with exertion, not to miss meals and to keep well hydrated. She was then referred to the Adult Metabolic Service and was placed on MCTs-rich diet. Conclusion: Fatty acid oxidation metabolism defect should be considered as a possible aetiology of exertional rhabdomyolysis in an appropriate clinical setting. Metabolic disorders are often underdiagnosed, and increased awareness can lead to early diagnosis and significant improvement in outcomes.L6328011342020-09-15 <br />en
dc.language.isoenen
dc.relation.ispartofInternal Medicine Journalen
dc.titleExertional rhabdomyolysis as a clinical manifestation of fatty acid oxidation metabolism defecten
dc.typeArticleen
dc.identifier.doi10.1111/imj.14849en
dc.subject.keywordsearly diagnosisen
dc.subject.keywordsexerciseen
dc.subject.keywordsfamily historyen
dc.subject.keywordsfastingen
dc.subject.keywordsfatty acid oxidationen
dc.subject.keywordsfemaleen
dc.subject.keywordsglucose intakeen
dc.subject.keywordshumanen
dc.subject.keywordshuman cellen
dc.subject.keywordshuman tissueen
dc.subject.keywordshydrationen
dc.subject.keywordslow fat dieten
dc.subject.keywordsmetabolic disorderen
dc.subject.keywordsmyalgiaen
dc.subject.keywordsrhabdomyolysisen
dc.subject.keywordsside effecten
dc.subject.keywordsmaleen
dc.subject.keywordsacylcarnitinecarbohydrateen
dc.subject.keywordsclomifeneen
dc.subject.keywordsendogenous compounden
dc.subject.keywordsessential fatty aciden
dc.subject.keywordsmedium chain triacylglycerolen
dc.subject.keywordsphosphotransferaseen
dc.subject.keywordsadulten
dc.subject.keywordsadverse drug reactionen
dc.subject.keywordsavoidance behavioren
dc.subject.keywordsawarenessen
dc.subject.keywordsbrotheren
dc.subject.keywordscase reporten
dc.subject.keywordschilden
dc.subject.keywordschildhooden
dc.subject.keywordsclinical articleen
dc.subject.keywordsconference abstracten
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L632801134&from=exporthttp://dx.doi.org/10.1111/imj.14849 |en
dc.identifier.risid1457en
dc.description.pages19en
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Sites:Children's Health Queensland Publications
Queensland Health Publications
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