Searchable abstracts of presentations at key conferences in endocrinology

ea0056gp123 | Endocrine Case Reports | ECE2018

A rare case of type-2 familial partial lipodystrophy (FLD type 2) non-Dunnigan type with laminin A/C gene (LMNA) mutation causing multi-organ failure and diabetes mellitus

Frunza-Stefan Simona , Memon Raafia , Malek Rana , Streeten Elizabeth , Pollin Toni , Silver Kristi

Introduction: Mutations of the LMNA gene cause a wide range of diseases including lipodystrophy, myopathy [including dilated cardiomyopathy (DCM)], neuropathy and progeroid syndrome, and are collectively known as A-type laminopathies.Case report: A 51-year-old Caucasian male with history of heart, liver and kidney transplants was referred for evaluation and treatment of post-transplant diabetes. He was diagnosed with hypertriglyceridemia at age 38. At 43...