A Novel cause of Massive Hepatosplenomegaly with Fibrosis in two children: Transient Infantile Hypertriglyceridemia
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Published:2024-03
Issue:2
Volume:14
Page:101288
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ISSN:0973-6883
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Container-title:Journal of Clinical and Experimental Hepatology
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language:en
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Short-container-title:Journal of Clinical and Experimental Hepatology
Author:
Sharma ShrutiORCID,
Sharma Yash P.,
Mardi Kavita,
Agarwal Ayushi,
Surya Mukesh
Reference6 articles.
1. Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1;Basel-Vanagaite;Am J Hum Genet,2012
2. A compound heterozygous mutation in GPD1 causes hepatomegaly, steatohepatitis, and hypertriglyceridemia;Joshi;Eur J Hum Genet EJHG,2014
3. Methylglyoxal-induced fibronectin gene expression through Ras-mediated NADPH oxidase activation in renal mesangial cells;Ho;Nephrol Carlton Vic,2007
4. Distinct ontogenic patterns of overt and latent DGAT activities of rat liver microsomes;Waterman;J Lipid Res,2002
5. Transient infantile hypertriglyceridemia and hepatic steatosis in an infant with GPD1 mutation;Kumar;Indian J Pediatr,2021