Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene

Familial chylomicronemia syndrome (FCS) is a rare monogenic form of severe hypertriglyceridemia, caused by mutations in genes involved in triglyceride metabolism. Herein, we report the case of a Korean family ...

Source: BMC Endocrine Disorders - April 15, 2024 Category: Endocrinology Authors: Ka Young Kim, You Joung Heo, Jung Min Ko, Young Ah Lee, Choong Ho Shin, Chang Seok Ki and Yun Jeong Lee Tags: Case Report Source Type: research