| Literature DB >> 29128061 |
Nidhi P Goyal1, Jeffrey B Schwimmer2.
Abstract
Nonalcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver disease in children. Severe fibrosis and cirrhosis are potential consequences of pediatric NAFLD and can occur within a few years of diagnosis. Observations suggest that genetics may be a strong modifying factor in the presentation, severity, and natural history of the disease. There is increasing interest in determining at-risk populations based on genetics in the hope of finding genotypes that correlate to NAFLD phenotype. Ultimately, the hope is to be able to tailor therapeutics to genetic predispositions and decrease disease morbidity in children with NAFLD.Entities:
Keywords: Alanine aminotransferase; Children; Liver; Nonalcoholic steatohepatitis; Obesity; PNPLA3; Steatosis; TM6SF2
Mesh:
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Year: 2017 PMID: 29128061 PMCID: PMC5693307 DOI: 10.1016/j.cld.2017.08.002
Source DB: PubMed Journal: Clin Liver Dis ISSN: 1089-3261 Impact factor: 6.126