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Plasma exchange for homozygous familial hypercholesterolaemia: the Cape Town experience

✍ Scribed by Marais, A.David; Wood, Lucille; Firth, Jean C.; Hall, Jane M.; Jacobs, Peter

Book ID: 122743746
Publisher: Elsevier Science
Year: 1993
Tongue: English
Weight: 879 KB
Volume: 14
Category: Article
ISSN: 0955-3886
DOI: 10.1016/0955-3886(93)90004-E

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## Abstract Familial hypercholesterolemia (FH) is an autosomal dominant disease. Homozygous FH (HFH) manifests with severe hypercholesterolemia since birth (cholesterol levels >5–6 the upper normal limit), which, if untreated, leads to early onset accelerated atherosclerosis and premature coronary