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Next Generation Sequencing – a key tool for diagnosis of Familial Dyslipidemias

dc.contributor.authorMiranda, B.
dc.contributor.authorAlves, A.C.
dc.contributor.authorBourbon, M.
dc.date.accessioned2023-11-28T14:49:57Z
dc.date.available2023-11-28T14:49:57Z
dc.date.issued2022-12-10
dc.description.abstractDyslipidemia, a clinical condition defined by abnormal lipid concentrations in blood, can have a genetic etiology. Familial dyslipidemias are a group of genetic diseases, the majority being rare, associated with several serious conditions. Raised triglyceride levels are associated with pancreatic/hepatic complications. Elevated cholesterol levels promote atherosclerosis and increase patients' cardiovascular risk, and low levels of this particle are associated with neurological manifestations and poor weight progression. Nowadays, with the advance in genome sequencing technologies, the investigation and diagnosis of these disorders is expandingpt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/8792
dc.language.isoengpt_PT
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpt_PT
dc.subjectFamilial Dyslipidemiaspt_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.titleNext Generation Sequencing – a key tool for diagnosis of Familial Dyslipidemiaspt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlacePeniche, Portugalpt_PT
oaire.citation.title4ª Reunião do Núcleo de Estudos de Prevenção e Risco Vascular, 10 december 2022pt_PT
rcaap.rightsclosedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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