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Familial chylomicronemia syndrome in Portugal

dc.contributor.authorAlves, Ana Catarina
dc.contributor.authorMiranda, Beatriz
dc.contributor.authorSequeira, Sílvia
dc.contributor.authorMoldovan, Oana
dc.contributor.authorNunes, Catarina
dc.contributor.authorAntunes, Henedina
dc.contributor.authorMartins, Esmeralda
dc.contributor.authorGonçalves, Rute
dc.contributor.authorDuarte, Sequeira
dc.contributor.authorGuerra, António
dc.contributor.authorGaspar, Ana
dc.contributor.authorSalgado, Miguel
dc.contributor.authorAzevedo, Aida
dc.contributor.authorAraújo, Francisco
dc.contributor.authorFerreira, Ana Cristina
dc.contributor.authorRato, Quitéria
dc.contributor.authorPalma, Isabel
dc.contributor.authorBourbon, Mafalda
dc.date.accessioned2022-07-08T16:28:27Z
dc.date.available2022-07-08T16:28:27Z
dc.date.issued2021-05
dc.description.abstractFamilial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder of lipoprotein metabolism. It is characterized by marked elevation of triglyceride and chylomicron levels, lipaemic plasma, recurrent pancreatitis, eruptive xanthoma, hepatosplenomegaly, andliapemiaretinalis. All genes associated with FCS (LPL, APOC2, APOA5, LMF1 and GPHBP1) have an effect on the activity of lipoprotein lipase (LPL). The aim of this study is to present all cases with FCS clinical diagnosis, studied in our laboratory.pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/8110
dc.language.isoengpt_PT
dc.subjectFamilial chylomicronemia Syndromept_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.subjectPortugalpt_PT
dc.titleFamilial chylomicronemia syndrome in Portugalpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboa, Portugal (online)pt_PT
oaire.citation.titleCurating the Clinical Genome Conference 2021, 12-14 maio 2021pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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