Key result
Whole-exome sequencing identified a novel homozygous variant, c.628 G > C:p.G210R, in the GPD1 gene as the cause of transient infantile hypertriglyceridemia in two siblings.
Why the study?
Transient infantile hypertriglyceridemia is a rare cause of unexplained elevated liver enzymes, hypertriglyceridemia, and hepatosteatosis that requires genetic diagnosis.
Case Report (n=2)
No
Whole exome sequencing is valuable for diagnosing unexplained childhood fatty liver disease and identifying novel GPD1 variants in transient infantile hypertriglyceridemia.
Transient infantile hypertriglyceridemia is one of the diseases that should be considered in case of unexplained elevated liver enzymes, hypertriglyceridemia and hepatosteatosis. We report 2 siblings with novel homozygous variants in the GPD1 gene with transient infantile hypertriglyceridemia. Two siblings born from consanguineous marriage were referred due to hepatomegaly, elevated transaminases and fatty liver. After excluding other possible causes of fatty liver and elevated transaminase levels; whole-exome sequencing (WES) was performed on genomic DNA isolated from the peripheral blood samples of both patients. Whole exome sequencing revealed the identification of a novel homozygous variant, c.628 G > C:p.G210R, in GPD1. Our report underscores the importance of genome sequencing in diagnosing unexplained childhood fatty liver disease and/or elevated enzyme levels. In patients with transient infantile hypertriglyceridemia, investigation into novel homozygous variants in the GPD1 gene should be conducted using whole exome sequencing.
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Belkaya et al. (2025) conducted a case report in Transient infantile hypertriglyceridemia (n=2). Homozygous variant c.628 G > C:p.G210R in GPD1 was evaluated on Identification of genetic variant. Whole-exome sequencing identified a novel homozygous variant, c.628 G > C:p.G210R, in the GPD1 gene as the cause of transient infantile hypertriglyceridemia in two siblings.
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