A Clinical Case of a Homozygous Deletion in the <i>APOA5</i> Gene with Severe Hypertriglyceridemia

A Clinical Case of a Homozygous Deletion in the <i>APOA5</i> Gene with Severe Hypertriglyceridemia

Background: Hypertriglyceridemia (HTG) is one of the most common forms of lipid metabolism disorders. The leading clinical manifestations are pancreatitis, atherosclerotic vascular lesions, and the formation of eruptive xanthomas. The most severe type of HTG is primary (or hereditary) hypertriglycer...

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Bibliographic Details
Main Authors: Petr Andreevich Vasiluev, Olga N. Ivanova, Natalia A. Semenova, Tatiana V. Strokova, Natalia N. Taran, Uliana V. Chubykina, Marat V. Ezhov, Ekaterina Y. Zakharova, Elena L. Dadli, Sergey I. Kutsev
Format: Article
Language:English
Published: MDPI AG 2022-06-01
Series:Genes
Subjects:
hypertriglyceridemia
pancreatitis
cardiovascular disease
<i>APOA5</i>
<i>LPL</i>
mutation
Online Access:https://www.mdpi.com/2073-4425/13/6/1062

Internet

https://www.mdpi.com/2073-4425/13/6/1062

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