Homozygous familial hypercholesterolemia

被引：1
|
作者：
Wierzbicki, Anthony S. [1 ,2 ]
机构：
[1] Guys Hosp, London SE1 7EH, England
[2] St Thomas Hosp, London SE1 7EH, England
来源：
CLINICAL LIPIDOLOGY | 2013年 / 8卷 / 04期
关键词：
antisense oligonucleotide; apheresis; coronary artery disease; familial hypercholesterolemia; homozygous; microsomal transfer protein inhibitor; xanthoma; LIPOPROTEIN APHERESIS; EFFICACY; ATORVASTATIN; DIAGNOSIS; PROTEIN; TRIAL;
D O I：
10.2217/CLP.13.37
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
Evaluation of: Rocha VZ, Chacra AP, Salgado W et al. Extensive xanthomata and severe subclinical atherosclerosis in homozygous familial hypercholesterolemia. J. Am. Coll. Cardiol. 61(21), 2193 (2013).This paper evaluation summarizes a case report of homozygous familial hypercholesterolemia. The patient in this particular case presented with gross xanthomata, elevated LDL cholesterol and extant coronary arterial disease in early adulthood. The clinical diagnosis, physical signs and management of the condition are discussed and future treatment options for homozygous familial hypercholesterolemia are reviewed.
引用
收藏
页码：407 / 409
页数：3
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