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dc.rights.licenseopenen_US
hal.structure.identifierCHU Bordeaux
dc.contributor.authorLEBRETON, Louis
dc.contributor.authorGASCHIGNARD, Margaux
hal.structure.identifierCHU Bordeaux
dc.contributor.authorGUIBET, Claire
dc.contributor.authorLAMIREAU, Delphine
dc.contributor.authorROCHE, Sandrine
hal.structure.identifierCHU Bordeaux
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorRICHARD, Emmanuel
hal.structure.identifierCHU Bordeaux
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorGED, Cecile
hal.structure.identifierCHU Bordeaux
dc.contributor.authorMESLI, Samir
hal.structure.identifierCHU Bordeaux
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorREDONNET-VERNHE, Isabelle
dc.date.accessioned2023-11-09T13:30:57Z
dc.date.available2023-11-09T13:30:57Z
dc.date.issued2023-01-01
dc.identifier.issn2192-8304en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/184700
dc.description.abstractEnPrimary carnitine deficiency (PCD) is an inherited disease of fatty acid beta-oxidation with autosomal recessive inheritance. The disease manifests as metabolic decompensation with hypoketotic hypoglycaemia associated with cardiomyopathy, hepatomegaly, rhabdomyolysis, and seizures. Various outcomes are described from asymptomatic adults to dramatic sudden infant death syndrome cases. We present a severe case of PCD decompensation in an 18-week-old female. She presented with hypotonia, moaning, diarrhea, and vomiting at the pediatric emergency. Initially suspected as intracranial hypertension, the clinical condition evolved rapidly and caused a reversible cardiac arrest with profound hypoglycemia. Despite carnitine supplementation, she succumbed from cardiac arrhythmia and multivisceral failure 4 days after admission. The genetic analyses showed a PCD with biallelic pathogenic variants of gene. The case report is notable for the severity of the cardiac damage possibly favored by maternal carnitine deficiency during pregnancy. The analysis of previously published PCD cases highlights (i) the importance of having large access to emergency biochemical tests for early therapeutic care although the disease has unpredictable severity and (ii) the fact that the clinical outcome remains unpredictable if carnitine treatment is initiated late.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enCardiomyopathy
dc.subject.enChildren
dc.subject.enFatty oxidation
dc.subject.enPrimary carnitine deficiency
dc.title.enInfantile primary carnitine deficiency: A severe cardiac presentation unresponsive to carnitine supplementation.
dc.title.alternativeJIMD Repen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/jmd2.12346en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed36636599en_US
bordeaux.journalJIMD reportsen_US
bordeaux.page35-41en_US
bordeaux.volume64en_US
bordeaux.hal.laboratoriesMaladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04277343
hal.version1
hal.date.transferred2023-11-09T13:30:59Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=JIMD%20reports&rft.date=2023-01-01&rft.volume=64&rft.issue=1&rft.spage=35-41&rft.epage=35-41&rft.eissn=2192-8304&rft.issn=2192-8304&rft.au=LEBRETON,%20Louis&GASCHIGNARD,%20Margaux&GUIBET,%20Claire&LAMIREAU,%20Delphine&ROCHE,%20Sandrine&rft.genre=article


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