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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...

Täydet tiedot

Tallennettuna:
Päätekijät: Johns T Johnson, Jinson Paul, Kripa Elizabeth Cherian, Nitin Kapoor, H S Asha, Thomas Vizhalil Paul
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Wolters Kluwer Medknow Publications 2020-01-01
Sarja:Journal of Family Medicine and Primary Care
Aiheet:
familial hypercholesterolemia
lipid disorder
tendon xanthoma
Linkit:http://www.jfmpc.com/article.asp?issn=2249-4863;year=2020;volume=9;issue=8;spage=4451;epage=4453;aulast=Johnson
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