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We present a case of pediatric onset chronic intestinal pseudoobstruction associated with a novel missense ACTG2 mutation c.439G&gt;T\/p.G147C. In addition to the known disease manifestations of feeding intolerance and intestinal malrotation, our patient had a late-onset hypertrophic pyloric stenosis and a late-onset choledochal cyst, the former of which has not previously been described in patients with ACTG2-associated visceral myopathy.<\/jats:p>","DOI":"10.1177\/1066896918786586","type":"journal-article","created":{"date-parts":[[2018,7,18]],"date-time":"2018-07-18T16:59:28Z","timestamp":1531933168000},"page":"77-83","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":21,"title":["<i>ACTG2<\/i>\n                    -Associated Visceral Myopathy With Chronic Intestinal Pseudoobstruction, Intestinal Malrotation, Hypertrophic Pyloric Stenosis, Choledochal Cyst, and a Novel Missense Mutation"],"prefix":"10.1177","volume":"27","author":[{"given":"Rebecca R. 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