Familial hypercholesterolemia: The skin speaks

Familial hypercholesterolaemia (FH) is an autosomal dominant inherited disorder of lipoprotein metabolism caused by defects in the low-density lipoprotein receptor (LDLR) gene. It is characterized by high low-density lipoprotein (LDL) cholesterol levels, premature cardiovascular disease (CVD), and t...

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Detalles Bibliográficos
Autores principales: Johnson, Johns T., Paul, Jinson, Cherian, Kripa Elizabeth, Kapoor, Nitin, Asha, H. S., Paul, Thomas Vizhalil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586528/
https://www.ncbi.nlm.nih.gov/pubmed/33110883
http://dx.doi.org/10.4103/jfmpc.jfmpc_819_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586528/
https://www.ncbi.nlm.nih.gov/pubmed/33110883
http://dx.doi.org/10.4103/jfmpc.jfmpc_819_20

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