Management of homozygous familial hypercholesterolaemia in two brothers

Homozygous familial hypercholesterolaemia (HoFH) is a rare, genetic disorder of abnormally high levels of low-density lipoprotein cholesterol (LDL-C) requiring aggressive interventions to retard the evolution of atherosclerotic cardiovascular disease. We treated two brothers (ages 46 years and 47 ye...

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Detalles Bibliográficos
Autores principales: Real, José, Arbona, Cristina, Goterris, Rosa, Ascaso, Juan Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Rare Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775811/
https://www.ncbi.nlm.nih.gov/pubmed/29306853
http://dx.doi.org/10.1136/bcr-2017-222155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775811/
https://www.ncbi.nlm.nih.gov/pubmed/29306853
http://dx.doi.org/10.1136/bcr-2017-222155

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