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Article

The enigma of persistent hypertriglyceridemia: A Case Report

2021-07-26

Abstract excerpt

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).

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Literature Corpus work
ddff6a4a-8bd2-5258-9bbc-4944924cd12a
DOI
10.22541/au.162728085.56631208/v1
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The enigma of persistent hypertriglyceridemia: A Case ReportDOI 10.22541/au.162728085.56631208/v1
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