The enigma of persistent hypertriglyceridemia: A case report.

Autor: Dhaliwal, Armaan, Ravi, Soumiya, Bains, Kanwal, Potharaju, Anil Kumar, Shah, Tasneem
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Zdroj: Clinical Case Reports; Mar2022, Vol. 10 Issue 3, p1-6, 6p
Abstrakt: 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. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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