A Model of Care for Familial Hypercholesterolaemia: Key Role for Clinical Biochemistry

Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth that causes marked elevation in plasma low-density lipoprotein (LDL) cholesterol concentrations and premature coronary heart disease. There are at least 45,000 people with FH in Australia and New Zealand, but m...

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Detalhes bibliográficos
Main Authors: Watts, Gerald F, Sullivan, David R, van Bockxmeer, Frank M, Poplawski, Nicola, Hamilton-Craig, Ian, Clifton, Peter M, O’Brien, Richard C, George, Peter M, Burnett, John R
Formato: Artigo
Idioma:Inglês
Publicado em: The Australian Association of Clinical Biochemists 2012
Assuntos:
Commentary
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3284341/
https://ncbi.nlm.nih.gov/pubmed/22363096
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