{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,13]],"date-time":"2025-05-13T14:21:38Z","timestamp":1747146098743,"version":"3.40.5"},"reference-count":20,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2022,12,21]],"date-time":"2022-12-21T00:00:00Z","timestamp":1671580800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2023,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>CHARGE syndrome is a malformation disorder with diverse phenotypes that shows autosomal dominance with heterozygous variants in the chromodomain helicase DNA\u2010binding 7 (<jats:italic>CHD7<\/jats:italic>) gene. Only a few cases of CHARGE syndrome accompanied by neoplasm during childhood have been reported. We report the case of a girl with CHARGE syndrome who developed acute myelogenous leukemia at 12\u2009years old. She had mild intellectual disability, and hearing loss with inner ear malformation, myopia, astigmatism, laryngotracheal malacia, hypogonadism, and clival hypoplasia, with a history of patent ductus arteriosus. The patient was genetically diagnosed with CHARGE syndrome based on the detection of a novel heterozygous frameshift pathogenic variant in the <jats:italic>CHD7<\/jats:italic> gene. We review the reported pediatric cases of CHARGE syndrome with malignancy and suggest a possible molecular mechanism of carcinogenesis involving pathogenic variants of the <jats:italic>CHD7<\/jats:italic> gene.<\/jats:p>","DOI":"10.1002\/ajmg.a.63087","type":"journal-article","created":{"date-parts":[[2022,12,21]],"date-time":"2022-12-21T23:23:35Z","timestamp":1671665015000},"page":"878-881","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Acute myeloid leukemia associated with <scp>CHARGE<\/scp> syndrome"],"prefix":"10.1002","volume":"191","author":[{"given":"Marie","family":"Shuto","sequence":"first","affiliation":[{"name":"Department of Pediatrics Oita University, Faculty of Medicine  Yufu Oita Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Naoki","family":"Hirano","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Oita University, Faculty of Medicine  Yufu Oita Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Saori","family":"Oguri","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Oita University, Faculty of Medicine  Yufu Oita Japan"},{"name":"Division of General Pediatrics and Emergency Medicine, Department of Pediatrics Oita University, Faculty of Medicine  Yufu Oita Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4894-5356","authenticated-orcid":false,"given":"Tomoyo","family":"Itonaga","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Oita University, Faculty of Medicine  Yufu Oita Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masanori","family":"Inoue","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Oita University, Faculty of Medicine  Yufu Oita Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Souichi","family":"Suenobu","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Oita University, Faculty of Medicine  Yufu Oita Japan"},{"name":"Division of General Pediatrics and Emergency Medicine, Department of Pediatrics Oita University, Faculty of Medicine  Yufu Oita Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8831-1991","authenticated-orcid":false,"given":"Kenji","family":"Ihara","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Oita University, Faculty of Medicine  Yufu Oita Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2022,12,21]]},"reference":[{"key":"e_1_2_9_2_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00381-019-04433-4"},{"key":"e_1_2_9_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jtho.2016.12.011"},{"key":"e_1_2_9_4_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.0905-6157.2003.00104.x"},{"key":"e_1_2_9_5_1","doi-asserted-by":"publisher","DOI":"10.1002\/1878-0261.12104"},{"key":"e_1_2_9_6_1","doi-asserted-by":"publisher","DOI":"10.1055\/s-0031-1275676"},{"key":"e_1_2_9_7_1","doi-asserted-by":"publisher","DOI":"10.1097\/ICO.0b013e31806c77d6"},{"key":"e_1_2_9_8_1","doi-asserted-by":"publisher","DOI":"10.3174\/ajnr.A1380"},{"key":"e_1_2_9_9_1","doi-asserted-by":"publisher","DOI":"10.3109\/08880018.2014.883002"},{"key":"e_1_2_9_10_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.37435"},{"key":"e_1_2_9_11_1","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.2003228117"},{"key":"e_1_2_9_12_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2559.2011.03819.x"},{"key":"e_1_2_9_13_1","doi-asserted-by":"publisher","DOI":"10.1038\/s41598-019-39564-w"},{"key":"e_1_2_9_14_1","doi-asserted-by":"publisher","DOI":"10.1089\/scd.2014.0544"},{"key":"e_1_2_9_15_1","doi-asserted-by":"publisher","DOI":"10.3390\/cancers13184586"},{"key":"e_1_2_9_16_1","doi-asserted-by":"publisher","DOI":"10.1136\/bcr.05.2009.1859"},{"key":"e_1_2_9_17_1","doi-asserted-by":"publisher","DOI":"10.1515\/jpem-2012-0162"},{"key":"e_1_2_9_18_1","doi-asserted-by":"publisher","DOI":"10.1038\/s41467-020-19502-5"},{"volume-title":"GeneReviews\u00ae [Internet]","year":"1993","author":"Ravenswaaij\u2010Arts C. 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