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

• Main Authors: Min-Huan Lin (Author), Xiao-Hui Tian (Author), Xiu-Lan Hao (Author), Hui Fei (Author), Jian-Lan Yin (Author), Dan-Dan Yan (Author), Tian Li (Author)
• Format: Book
• Published: BMC, 2020-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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....