GPD1 and transient infantile hypertriglyceridemia and hepatosteatosis: GPD1 mutations were first identified by Basel-Vanagaite et al. as the cause of transient infantile hypertriglyceridemia (HTGTI; OMIM 614480) in 10 individuals from four consanguineous Israeli Arab families carrying a homozygous founder mutation c.361-1G>C [3].