A Case of Familial Partial Lipodystrophy Type 3 with A Novel Pparg Variant of Unknown Significance
1. Abstract Familial partial lipodystrophy (FPLD) is a heterogeneous group of rare genetic disorders (estimated prevalence <1/100,000) characterized by a lipodystrophy phenotype combined with metabolic abnormalities such as insulin resistance and hypertriglyceridemia. Several subtypes have been described
