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The enigma of persistent hypertriglyceridemia: A case report
Armaan Dhaliwal1, Soumiya Ravi2, Kanwal Bains3
1University of Arizona College of Medicine at South Campus Tucson Arizona USA.
Abstract:
A patient with a history of Mandibular hypoplasia, Deafness, Progeroid Features Associated Lipodystrophy Syndrome (MDPL), familial lipodystrophy presented with hypertriglyceridemia induced pancreatitis with triglycerides in the 3000s. This lipodystrophy occurs due to a mutation in the POLD1 gene (DNA polymerase delta 1). MDPL, hypertriglyceridemia, pancreatitis, POLD1.
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