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The enigma of persistent hypertriglyceridemia: A Case Report
  • +2
  • Armaan Dhaliwal,
  • Soumiya Ravi,
  • Kanwal Naveen Bains,
  • Anil Potharaju,
  • Tasneem Shah
Armaan Dhaliwal
University of Arizona Medical Center - South Campus
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Soumiya Ravi
Dayanand Medical College and Hospital
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Kanwal Naveen Bains
Roger Williams Medical Center
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Anil Potharaju
University of Arizona Medical Center - South Campus
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Tasneem Shah
University of Arizona Medical Center - South Campus
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Abstract

A patient with a history of Mandibular hypoplasia, Deafness, Progeroid Features Associated Lipodystrophy Syndrome (MDPL), a 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).

Peer review status:IN REVISION

23 Jul 2021Submitted to Clinical Case Reports
24 Jul 2021Assigned to Editor
24 Jul 2021Submission Checks Completed
26 Jul 2021Reviewer(s) Assigned
06 Sep 2021Review(s) Completed, Editorial Evaluation Pending
09 Sep 2021Editorial Decision: Revise Minor