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Portuguese Familial Hypercholesterolemia Study: presentation of the study and preliminary results

dc.contributor.authorBourbon, M.
dc.contributor.authorRato, Q.
dc.contributor.authorInvestigadores do Estudo Português de Hipercolesterolemia Familiar
dc.date.accessioned2011-11-30T17:08:10Z
dc.date.available2011-11-30T17:08:10Z
dc.date.issued2006-11-06
dc.description.abstractFamilial hypercholesterolemia (FH) is an autosomal dominant genetic disorder caused, in the majority of cases, by a partial or total lack of functional low density lipoprotein receptors (LDLR). Mutations in the LDLR gene lead to increased plasma cholesterol levels, resulting in cholesterol deposition in the arteries, thereby increasing the risk of premature coronary heart disease. The homozygous form of FH is rare but heterozygous FH is common, although underdiagnosed in many populations, including the Portuguese. In 1999 the Portuguese Familial Hypercholesterolemia Study was begun at the National Institute of Health.por
dc.identifier.citationRev Port Cardiol. 2006 Nov;25(11):999-1013.por
dc.identifier.issn0870-2551
dc.identifier.urihttp://hdl.handle.net/10400.18/325
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherSociedade Portuguesa de Cardiologiapor
dc.relation.publisherversionhttp://www.spc.pt/DL/RPC/artigos/771.pdfpor
dc.subjectFamilial hypercholesterolemiapor
dc.subjectGenetic diagnosispor
dc.subjectLow-density lipoprotein receptorpor
dc.subjectMutationpor
dc.subjectCoronary heart diseasepor
dc.subjectIndex casepor
dc.subjectDoenças Cardio e Cérebro-vascularespor
dc.titlePortuguese Familial Hypercholesterolemia Study: presentation of the study and preliminary resultspor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage1013por
oaire.citation.startPage999por
oaire.citation.titleRevista Portuguesa de Cardiologiapor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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