Familial chylomicronemia syndrome

被引：28

作者：

Sugandhan, Selvendran ^{[1
]}

Khandpur, Sujay ^{[1
]}

Sharma, Vinod K. ^{[1
]}

机构：

[1] All India Inst Med Sci, Dept Dermatol & Venerol, New Delhi 110029, India

来源：

PEDIATRIC DERMATOLOGY | 2007年 / 24卷 / 03期

关键词：

D O I：

10.1111/j.1525-1470.2007.00415.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Familial chylomicronemia syndrome is a rare disorder of lipoprotein metabolism due to familial lipoprotein lipase (LPL) or apolipoprotein C-II deficiency or the presence of inhibitors to lipoprotein lipase. It manifests as eruptive xanthomas, acute pancreatitis, and lipaemic plasma due to marked elevation of triglyceride and chylomicron levels. We report two siblings with this rare disorder and review the literature.

引用

页码：323 / 325

页数：4

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