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Cascade Screening in Familial Hypercholesterolemia importance in early detection

dc.contributor.authorLeitão, F.
dc.contributor.authorMedeiros, A.M.
dc.contributor.authorBerguete, S.
dc.contributor.authorAlves, A.C.
dc.contributor.authorBourbon, M.
dc.date.accessioned2013-02-11T16:34:22Z
dc.date.available2013-02-11T16:34:22Z
dc.date.issued2012-11
dc.descriptionAna Margarida Medeiros was funded by Portuguese Society of Cardiology; Ana Catarina Alves was funded by FCT SFRH / BD / 27990 / 2006; project grant FCT_PTDC/SAU-GMG/101874/2008; project grant FCT PIC/IC/83333/2007; project grant from Portuguese Society of Cardiology 2006-2009 and 2010-2012 Porto, November 2012por
dc.description.abstractFamilial hypercholesterolemia (FH) is a genetic condition mainly caused by mutations in LDLR but missense mutations in APOB and PCSK9 can cause similar phenotypes. FH is characterized by increased levels of LDL cholesterol, leading to premature cardiovascular diseases (CVD). Cascade screening (CS) allows the rapid identification of new FH cases within a family. The main goal of this work is to perform CS of FH families and to understand the importance of this approach to identify prematurely individuals that are at risk to develop CVD.por
dc.identifier.urihttp://hdl.handle.net/10400.18/1251
dc.language.isoengpor
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpor
dc.subjectDoenças Cardio e Cérebro-vascularespor
dc.titleCascade Screening in Familial Hypercholesterolemia importance in early detectionpor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlacePorto, Portugalpor
oaire.citation.title16ª Reunião Anual da Sociedade Portuguesa de Genética Humana, 22-24 Novembro 2012por
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor

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