Case of homozygous familial hypercholesterolaemia with premature coronary artery disease

Familial hypercholesterolaemia is a genetic disorder secondary to mutation of one or more of the genes critical for low-density lipoprotein cholesterol (LDL-C) metabolism; these mutation(s) cause highly elevated serum LDL-C, significantly increasing the risk of early cardiovascular events and mortal...

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Dades bibliogràfiques
Publicat a:BMJ Case Rep
Autors principals: Suresh Kumar, Gayatri, Mathbout, Mohammad F, Fahsah, Ibrahim, Ghafghazi, Shahab
Format: Artigo
Idioma:Inglês
Publicat: BMJ Publishing Group 2021
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8137257/
https://ncbi.nlm.nih.gov/pubmed/34011640
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2021-242114
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