Transient Infantile Hypertriglyceridemia and Hepatic Steatosis in an Infant with GPD1 Mutation
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DOI: 10.1007/s12098-021-03663-2
Abstract: To the Editor: Transient infantile hypertriglyceridemia is a rare autosomal recessive disorder [1]. Till date, 27 patients with this disorder have been described with homozygous or compound heterozygous mutations in glycerol-3-phosphate dehydrogenase-1 (GPD1) [2]. To… read more here.
Keywords: hypertriglyceridemia; infantile hypertriglyceridemia; transient infantile; gpd1 ... See more keywords