{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,4,9]],"date-time":"2025-04-09T00:48:34Z","timestamp":1744159714811,"version":"3.37.3"},"reference-count":11,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2017,6,21]],"date-time":"2017-06-21T00:00:00Z","timestamp":1498003200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2017,9]]},"abstract":"<jats:sec><jats:label\/><jats:p>Xq25q26 duplication syndrome has been reported in individuals with clinical features such as short stature, intellectual disability, syndromic facial appearance, small hands and feet, and genital abnormalities. The symptoms are related to critical chromosome regions including Xq26.1\u201026.3. In this particular syndrome, no patient with congenital heart disease was previously reported. Here, we report a 6\u2010year\u2010old boy with typical symptoms of Xq25q26 duplication syndrome and double outlet right ventricle (DORV) with pulmonary atresia (PA). He had the common duplicated region of Xq25q26 duplication syndrome extending to the distal region including the <jats:italic>MOSPD1<\/jats:italic> locus. MOSPD1 regulates transforming growth factor beta (TGF\u03b2) 2,3 and may be responsible for cardiac development including DORV. In the patient's lymphocytes, mRNA expression of <jats:italic>TGF\u03b22<\/jats:italic> was lower than control, and might cause DORV as it does in <jats:italic>TGF\u03b22<\/jats:italic>\u2010deficient mice. Therefore, <jats:italic>MOSPD1<\/jats:italic> is a possible candidate gene for DORV, probably in combination with <jats:italic>GPC3<\/jats:italic>. Further studies of the combined functions of MOSPD1 and GPC3 are needed, and identification of additional patients with <jats:italic>MOSPD1<\/jats:italic> and <jats:italic>GPC3<\/jats:italic> duplication should be pursued.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ajmg.a.38297","type":"journal-article","created":{"date-parts":[[2017,6,21]],"date-time":"2017-06-21T10:52:36Z","timestamp":1498042356000},"page":"2446-2450","source":"Crossref","is-referenced-by-count":4,"title":["Xq26.1\u201026.3 duplication including MOSPD1 and GPC3 identified in boy with short stature and double outlet right ventricle"],"prefix":"10.1002","volume":"173","author":[{"given":"Yukiko","family":"Hirota","sequence":"first","affiliation":[{"name":"Department of Pediatrics Jichi Medical University Tochigi Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3821-2450","authenticated-orcid":false,"given":"Takaomi","family":"Minami","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Jichi Medical University Tochigi Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tomoyuki","family":"Sato","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Jichi Medical University Tochigi Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Akiko","family":"Yokomizo","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Jichi Medical University Tochigi Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Auimi","family":"Matsumoto","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Jichi Medical University Tochigi Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masahide","family":"Goto","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Jichi Medical University Tochigi Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eriko","family":"Jinbo","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Jichi Medical University Tochigi Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takanori","family":"Yamamgata","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Jichi Medical University Tochigi Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2017,6,21]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/S1359-6101(03)00044-3"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1158\/0008-5472.CAN-04-4244"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1038\/jhg.2010.119"},{"key":"e_1_2_5_5_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00439-013-1403-3"},{"key":"e_1_2_5_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ydbio.2009.08.029"},{"key":"e_1_2_5_7_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.2008.057984"},{"key":"e_1_2_5_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ygeno.2004.08.017"},{"key":"e_1_2_5_9_1","doi-asserted-by":"publisher","DOI":"10.1038\/ng0396-241"},{"key":"e_1_2_5_10_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.33227"},{"issue":"13","key":"e_1_2_5_11_1","doi-asserted-by":"crossref","first-page":"2659","DOI":"10.1242\/dev.124.13.2659","article-title":"TGF beta2 knockout mice have multiple developmental defects that are non\u2010overlapping with other TGF beta knockout phenotypes","volume":"124","author":"Sanford L. 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