Plasma signatures of Congenital Generalized Lipodystrophy patients identified by untargeted lipidomic profiling are not changed after a fat-containing breakfast meal

Congenital Generalized Lipodystrophy (CGL), also known as Berardinelli-Seip congenital lipodystrophy, is an autosomal recessive disorder characterized by severe loss of adipose tissue, approaching total tissue absence since birth or in early infancy [1]. Life expectancy is significantly shortened in CGL [2].
Source: Prostaglandins, Leukotrienes and Essential Fatty Acids - Category: Biomedical Science Authors: Source Type: research