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Specification of ACMG/AMP variant classification guidelines for Familial Hypercholesterolemia – a ClinGen FH Variant Curation Committee Pilot Study

dc.contributor.authorKurtz, C. Lisa
dc.contributor.authorCarrie, Alain
dc.contributor.authorChora, Joana R.
dc.contributor.authorIacocca, Michael
dc.contributor.authorLeigh, Sarah
dc.contributor.authorFreiberger, Tomas
dc.contributor.authorTichy, Lukas
dc.contributor.authorDefesche, Joep
dc.contributor.authorHegele, Robert
dc.contributor.authorSijbrands, Eric
dc.contributor.authorKnowles, Josh
dc.contributor.authorBourbon, Mafalda
dc.date.accessioned2019-03-04T12:12:52Z
dc.date.available2019-03-04T12:12:52Z
dc.date.issued2018-04
dc.description.abstractFamilial hypercholesterolemia (FH) is a common autosomal dominant disorder (~1:250 individuals affected) of lipid metabolism, associated with an increased risk of cardiovascular disease. Individuals with FH characteristically present with severely elevated blood cholesterol levels, which leads to atherosclerotic plaque formation and subsequently, myocardial infarction due to premature coronary artery disease. Three main causative genes have been associated with FH: LDLR, APOB and PCSK9. Diagnosis is critical for early intervention and treatment, and it is imperative that family members of affected individuals be identified as early as possible.pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/6044
dc.language.isoengpt_PT
dc.subjectFamilial Hypercholesterolemiapt_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.titleSpecification of ACMG/AMP variant classification guidelines for Familial Hypercholesterolemia – a ClinGen FH Variant Curation Committee Pilot Studypt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceCharlotte NC, USApt_PT
oaire.citation.titleACMG Annual Clinical Genetics Meeting, 10-14 april 2018pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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