The enigma of persistent hypertriglyceridemia: A case report.
Publication/Presentation Date
3-1-2022
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.
Volume
10
Issue
3
First Page
05610
Last Page
05610
ISSN
2050-0904
Published In/Presented At
Dhaliwal, A., Ravi, S., Bains, K., Potharaju, A. K., & Shah, T. (2022). The enigma of persistent hypertriglyceridemia: A case report. Clinical case reports, 10(3), e05610. https://doi.org/10.1002/ccr3.5610
Disciplines
Medicine and Health Sciences
PubMedID
35356184
Department(s)
Department of Medicine, Department of Medicine Fellows and Residents, Fellows and Residents
Document Type
Article
COinS