{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,8]],"date-time":"2025-11-08T12:11:59Z","timestamp":1762603919673},"reference-count":13,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2014,9,24]],"date-time":"2014-09-24T00:00:00Z","timestamp":1411516800000},"content-version":"vor","delay-in-days":54,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatrics International"],"published-print":{"date-parts":[[2014,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">X<\/jats:styled-content>\u2010linked alpha thalassemia mental retardation (<jats:styled-content style=\"fixed-case\">ATR<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">X<\/jats:styled-content>) syndrome is an <jats:styled-content style=\"fixed-case\">X<\/jats:styled-content>\u2010linked recessive disorder that often involves gastrointestinal symptoms. Aspiration pneumonia related to gastroesophageal reflux has been reported as the major cause of death, but gastrointestinal function has not been well investigated. The present report describes a child with <jats:styled-content style=\"fixed-case\">ATR<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">X<\/jats:styled-content> syndrome who suffered from periodical episodes of refractory vomiting. We investigated the function of upper alimentary tract and found that esophago\u2010gastric dysmotility and severe gastric volvulus were the major causes of gastrointestinal symptoms. This child was surgically treated with anterior gastropexy and jejunal alimentation through gastrostomy, and the symptoms were relieved with good weight gain. This report may provide insight into the gastrointestinal function and nutritional management in children with <jats:styled-content style=\"fixed-case\">ATR<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">X<\/jats:styled-content> syndrome.<\/jats:p>","DOI":"10.1111\/ped.12402","type":"journal-article","created":{"date-parts":[[2014,9,24]],"date-time":"2014-09-24T06:25:25Z","timestamp":1411539925000},"source":"Crossref","is-referenced-by-count":6,"title":["Esophago\u2010gastric motility and nutritional management in a child with <scp>ATR<\/scp>\u2010<scp>X<\/scp> syndrome"],"prefix":"10.1111","volume":"56","author":[{"given":"Toshihiko","family":"Watanabe","sequence":"first","affiliation":[{"name":"Department of Surgical Subspecialties Division of Surgery National Center for Child Health and Development  Tokyo Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Katsuhiro","family":"Arai","sequence":"additional","affiliation":[{"name":"Department of Medical Subspecialties Division of Gastroenterology National Center for Child Health and Development  Tokyo Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masataka","family":"Takahashi","sequence":"additional","affiliation":[{"name":"Department of Surgical Subspecialties Division of Surgery National Center for Child Health and Development  Tokyo Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michinobu","family":"Ohno","sequence":"additional","affiliation":[{"name":"Department of Surgical Subspecialties Division of Surgery National Center for Child Health and Development  Tokyo Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kaori","family":"Sato","sequence":"additional","affiliation":[{"name":"Department of Surgical Subspecialties Division of Surgery National Center for Child Health and Development  Tokyo Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yasushi","family":"Fuchimoto","sequence":"additional","affiliation":[{"name":"Department of Surgical Subspecialties Division of Surgery National Center for Child Health and Development  Tokyo Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takahiko","family":"Wada","sequence":"additional","affiliation":[{"name":"Department of Medical Ethics\/Medical Genetics Kyoto University Graduate School of Medicine  Kyoto Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shinobu","family":"Ida","sequence":"additional","affiliation":[{"name":"Departments of Pediatrics Division of Gastroenterology, Nutrition and Endocrinology Osaka Medical Center and Research Institute for Maternal and Child Health  Osaka Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hisayoshi","family":"Kawahara","sequence":"additional","affiliation":[{"name":"Department of Pediatric Surgery Osaka Medical Center and Research Institute for Maternal and Child Health  Osaka Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yutaka","family":"Kanamori","sequence":"additional","affiliation":[{"name":"Department of Surgical Subspecialties Division of Surgery National Center for Child Health and Development  Tokyo Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2014,9,24]]},"reference":[{"key":"e_1_2_5_2_1","first-page":"1112","article-title":"Clinical features and molecular analysis of the alpha thalassemia\/mental retardation syndromes. 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