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3 articles related to "Familial Hypertriglyceridemia"

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Articles

Original Research

Published on 20 May 2022

The Genetic Spectrum of Familial Hypertriglyceridemia in Oman

in Genetics of Common and Rare Diseases

Khalid Al-Waili
Khalid Al-Rasadi
Muna Al-Bulushi
Mohammed Habais
Abdullah Al-Mujaini
Saif Al-Yaarubi
Antoine Rimbert
Razan Zadjali
Pegah Moradi Khaniabadi
Hamida Al-Barwani

Frontiers in Genetics

doi 10.3389/fgene.2022.886182

5,178 views
6 citations

Case Report

Accepted on 11 Feb 2026

Case report: Genetic testing reveals Wilson disease with familial hypertriglyceridemia in a 12-year-old boy

in Pediatric Gastroenterology, Hepatology and Nutrition

Yuemiao Wang
Daren Wu
Dandan Sun
Jiawei Wang
Xun Wang

Frontiers in Pediatrics

Original Research

Published on 16 Mar 2022

A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia

in Genetics of Common and Rare Diseases

Danxia Guo
Yingchun Zheng
Zhongzhi Gan
Yingying Guo
Sijie Jiang
Fang Yang
Fu Xiong
Hua Zheng

Frontiers in Genetics

doi 10.3389/fgene.2022.814295

4,132 views
6 citations