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Genetics of the monogenic forms of dyslipidaemia
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| 2.33 MB | Adobe PDF |
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Orientador(es)
Resumo(s)
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.
Descrição
Palavras-chave
Familial Hypercholesterolemia Sitosterolaemia Portuguese FH study Personalized Medicine Dyslipidaemia Doenças Cardio e Cérebro-vasculares