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dc.contributor.authorHaka, D.
dc.contributor.authorCekmen, N.
dc.date.accessioned2024-07-26T12:08:28Z
dc.date.available2024-07-26T12:08:28Z
dc.date.issued2023
dc.identifier.issn2220-1181en_US
dc.identifier.urihttps://journals.co.za/doi/epdf/10.36303/SAJAA.2987
dc.identifier.urihttp://hdl.handle.net/11727/12162
dc.description.abstractGlycogen storage disease (GSD) type III is a metabolic disorder caused by a deficiency in amylo-1,6-glucosidase enzyme, which is responsible for the breakdown of the glycogen molecule, resulting in glycogen accumulating in the organs, hypoglycaemia, muscle weakness, liver dysfunction, delayed anaesthetic recovery, excessive surgical bleeding, cardiomyopathy and end-organ dysfunction. This case report presents a child with GSD type IIIa who underwent orthotopic liver transplantation (OLT) with her mother as a donor. A multidisciplinary approach should be provided to optimise the preoperative period and minimise complications in these patients.en_US
dc.language.isoengen_US
dc.relation.isversionof10.36303/SAJAA.2987en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectanaesthetic managementen_US
dc.subjectglycogen storage diseaseen_US
dc.subjecttight glycaemic controlen_US
dc.subjecthypoglycaemiaen_US
dc.subjectliver transplantationen_US
dc.titleAnaesthetic Management for Orthotopic Liver Transplantation in A Patient with Glycogen Storage Disease Type Iiiaen_US
dc.typearticleen_US
dc.relation.journalSOUTHERN AFRICAN JOURNAL OF ANAESTHESIA AND ANALGESIAen_US
dc.identifier.volume29en_US
dc.identifier.issue5en_US
dc.identifier.startpage184en_US
dc.identifier.endpage186en_US
dc.identifier.wos001089490500005en_US
dc.identifier.scopus2-s2.0-85174913043en_US
dc.identifier.eissn2220-1173en_US
dc.contributor.orcID0000-0001-7448-8203en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US


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