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The enigma of persistent hypertriglyceridemia: A Case Report
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  • Armaan Dhaliwal,
  • Soumiya Ravi,
  • Kanwal Naveen Bains,
  • Anil Potharaju,
  • Tasneem Shah
Armaan Dhaliwal
University of Arizona Medical Center - South Campus

Corresponding Author:[email protected]

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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:Published

23 Jul 2021Submitted to Clinical Case Reports
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24 Jul 2021Submission Checks Completed
24 Jul 2021Assigned to Editor
26 Jul 2021Reviewer(s) Assigned
06 Sep 2021Review(s) Completed, Editorial Evaluation Pending
09 Sep 2021Editorial Decision: Revise Minor
06 Oct 20211st Revision Received
06 Oct 2021Assigned to Editor
06 Oct 2021Submission Checks Completed
06 Oct 2021Review(s) Completed, Editorial Evaluation Pending
10 Oct 2021Reviewer(s) Assigned
06 Nov 2021Editorial Decision: Revise Minor
24 Nov 20212nd Revision Received
28 Dec 2021Assigned to Editor
28 Dec 2021Submission Checks Completed
28 Dec 2021Review(s) Completed, Editorial Evaluation Pending
01 Jan 2022Reviewer(s) Assigned
30 Jan 2022Editorial Decision: Accept
Mar 2022Published in Clinical Case Reports volume 10 issue 3. 10.1002/ccr3.5610