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A Clinical Case of a Homozygous Deletion in the APOA5 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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Detalles Bibliográficos
Autores principales:	Vasiluev, Petr Andreevich, Ivanova, Olga N., Semenova, Natalia A., Strokova, Tatiana V., Taran, Natalia N., Chubykina, Uliana V., Ezhov, Marat V., Zakharova, Ekaterina Y., Dadli, Elena L., Kutsev, Sergey I.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222921/ https://www.ncbi.nlm.nih.gov/pubmed/35741823 http://dx.doi.org/10.3390/genes13061062

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