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Sitosterolaemia: a case of rare hypercholesterolaemia in FH patient’s cohort

dc.contributor.authorAlves, Ana Catarina
dc.contributor.authorMedeiros, Ana
dc.contributor.authorPadeira, Gonçalo
dc.contributor.authorFerreira, Ana Cristina
dc.contributor.authorBourbon, Mafalda
dc.date.accessioned2017-11-03T16:27:05Z
dc.date.available2017-11-03T16:27:05Z
dc.date.issued2017-04
dc.description.abstractAims: Familial Hyperpercholesterolaemia (FH) is the most common of all genetic hypercholesterolaemias. However there are other rare disorders presenting the same phenotype (phenocopies). Sitosterolaemia is one of those rare recessive disorders in which patients can present high levels of LDL-C but, most importantly, they present vegetal fat accumulation in tendons and arteries, leading also to increased cardiovascular risk. The defect in this case is in transporter genes responsible for the intestinal and biliary transport of plant sterols (ABCG5/ABCG8). AIMS: to identify the genetic cause of hypercholesterolaemia in a clinical FH patient presenting a severe phenotype.pt_PT
dc.description.sponsorshipWork supported by centre grant (to BioISI, Centre Reference: UID/MULTI/04046/2013), from FCT/MCTES/PIDDAC, Portugal.pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/4813
dc.language.isoengpt_PT
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpt_PT
dc.subjectSitosterolaemiapt_PT
dc.subjectFamilial Hyperpercholesterolaemiapt_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.titleSitosterolaemia: a case of rare hypercholesterolaemia in FH patient’s cohortpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FMulti%2F04046%2F2013/PT
oaire.citation.conferencePlacePraga, República Checapt_PT
oaire.citation.titleEuropean Atherosclerosis Society (EAS), 23-26 abril 2017pt_PT
oaire.fundingStream5876
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isProjectOfPublicationdc84f768-e6f2-4eea-b294-6c8ebbd1a156
relation.isProjectOfPublication.latestForDiscoverydc84f768-e6f2-4eea-b294-6c8ebbd1a156

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