Genetics of the monogenic forms of dyslipidaemia

Familial hypercholesterolemia (FH) is an autosomal dominant disorder associated with high levels of LDL-c and premature CHD (pCHD). Identification of FH in pediatric age is essential for a timely diagnosis and management. This study aims to highlight the importance of FH diagnosis in children.

Detalhes bibliográficos
Autor principal: Bourbon, Mafalda (author)
Formato: conferenceObject
Idioma:eng
Publicado em: 2019
Assuntos:
Familial Hypercholesterolemia
Sitosterolaemia
Portuguese FH study
Personalized Medicine
Dyslipidaemia
Doenças Cardio e Cérebro-vasculares
Texto completo:http://hdl.handle.net/10400.18/6432
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/6432

Texto Completo

http://hdl.handle.net/10400.18/6432

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