Management of a pregnant patient with chylomicronemia from a novel mutation in GPIHBP1: a case report.
Min-Huan LinXiao-Hui TianXiu-Lan HaoHui FeiJian-Lan YinDan-Dan YanTian LiPublished in: BMC pregnancy and childbirth (2020)
The case report contributes to the understanding of GPIHBP1-deficient familial chylomicronemia syndrome (FCS) and highlights gestational management of FCS patient.