Management of a pregnant patient with chylomicronemia from a novel mutation in GPIHBP1: a case report

Management of a pregnant patient with chylomicronemia from a novel mutation in GPIHBP1: a case report

Abstract Background Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive lipid disorder often associated with recurrent episodes of pancreatitis. It is documented in most cases with FCS due to the mutations of key proteins in lipolysis, including LPL, APOC2, APOA5, LMF1 and GPIHBP1....

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Bibliographic Details
Main Authors: Min-Huan Lin, Xiao-Hui Tian, Xiu-Lan Hao, Hui Fei, Jian-Lan Yin, Dan-Dan Yan, Tian Li
Format: Article
Language:English
Published: BMC 2020-05-01
Series:BMC Pregnancy and Childbirth
Subjects:
GPIHBP1
Chylomicronemia
Hypertriglyceridemia
Pancreatitis
Pregnancy
Online Access:http://link.springer.com/article/10.1186/s12884-020-02965-1

Internet

http://link.springer.com/article/10.1186/s12884-020-02965-1

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