A homozygous variant in the gpihbp1 gene in a child with severe hypertriglyceridemia and a systematic literature review

HIGHLIGHTS

• who: August et al. from the Kanazawa University, Japan have published the research: A homozygous variant in the GPIHBP1 gene in a child with severe hypertriglyceridemia and a systematic literature review, in the Journal: (JOURNAL) of 11/06/2022

SUMMARY

Of type I hyperlipoproteinemia because of a pathogenic variant in the GPIHBP1 is estimated between 1:500,000 to 1:1,000,000 (Gonzaga-Jauregui et_al, 2014). Affecting 15-20% of the population (Parhofer and Laufs, 2019; Basit et_al, 2020), hypertriglyceridemia has been associated with an increased risk for pancreatitis (Carrasquilla et_al; Simha . . .

 



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