| Literature DB >> 25688481 |
Don Hayes1, Patrick S Warren, Karen S McCoy, Shahid I Sheikh.
Abstract
Treatment of liver disease, including hepatic steatosis, in patients with cystic fibrosis (CF) is limited. With the development of ivacaftor, which corrects the gating defect of the CF transmembrane regulator channel, there is a potential new therapy available for this subgroup of the CF patient population. We present an adolescent with CF who had significant improvement in hepatic steatosis with ivacaftor treatment while hypothesizing on a mechanism of why it occurred.Entities:
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Year: 2015 PMID: 25688481 DOI: 10.1097/MPG.0000000000000765
Source DB: PubMed Journal: J Pediatr Gastroenterol Nutr ISSN: 0277-2116 Impact factor: 2.839