{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,6,2]],"date-time":"2024-06-02T23:31:23Z","timestamp":1717371083529},"reference-count":14,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2014,12,10]],"date-time":"2014-12-10T00:00:00Z","timestamp":1418169600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Obstet and Gynaecol"],"published-print":{"date-parts":[[2015,4]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Congenital hallux varus is a rare deformity of the great toe characterized by adduction of the hallux and medial displacement of the first metatarsophalangeal joint. Prenatal diagnosis of congenital hallux varus is presented herein. A 32\u2010year\u2010old woman was referred to our unit due to significant deviation of the fetal right great toe at 22<jats:sup>+2<\/jats:sup> weeks of pregnancy. Ultrasound examination revealed a thick and short great toe, which was significantly angulated medially on the right side. Amniocentesis was performed and the result was reported as inv(9) (p11;q12). After delivery, the clinical examination confirmed the prenatal diagnosis. To our knowledge, this is the first reported prenatal diagnosis of an isolated congenital hallux varus. Congenital hallux varus can be diagnosed easily in the prenatal period by 2\u2010<jats:styled-content style=\"fixed-case\">D<\/jats:styled-content> and 4\u2010<jats:styled-content style=\"fixed-case\">D<\/jats:styled-content> ultrasonography. Prenatal karyotyping should be taken into consideration, especially in the presence of associated anomalies, such as polydactyly and clubfoot.<\/jats:p>","DOI":"10.1111\/jog.12603","type":"journal-article","created":{"date-parts":[[2014,12,10]],"date-time":"2014-12-10T10:49:13Z","timestamp":1418208553000},"page":"628-630","source":"Crossref","is-referenced-by-count":2,"title":["Prenatal diagnosis of congenital hallux varus deformity associated with pericentric inversion of chromosome 9"],"prefix":"10.1111","volume":"41","author":[{"given":"Sebahat","family":"Atar G\u00fcrel","sequence":"first","affiliation":[{"name":"Division of Perinatology Department of Obstetrics and Gynecology Maternity and Children's Hospital Ministry of Health and Medical School of Ordu University  Ordu Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2014,12,10]]},"reference":[{"key":"e_1_2_5_2_1","first-page":"277","article-title":"Hallux varus","volume":"15","author":"McElvenny RT","year":"1941","journal-title":"Q Bull Northwest Univ Med Sch"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1177\/107110079501600801"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1177\/107110078200300311"},{"key":"e_1_2_5_5_1","doi-asserted-by":"publisher","DOI":"10.1177\/107110078000100109"},{"key":"e_1_2_5_6_1","doi-asserted-by":"publisher","DOI":"10.1177\/107110078300300409"},{"key":"e_1_2_5_7_1","doi-asserted-by":"publisher","DOI":"10.1177\/107110079501600408"},{"key":"e_1_2_5_8_1","first-page":"563","article-title":"Hallux varus congenitus und polydaktylie","volume":"59","author":"Mestern J","year":"1933","journal-title":"Z Orthop"},{"key":"e_1_2_5_9_1","doi-asserted-by":"publisher","DOI":"10.4103\/0971-3026.63044"},{"key":"e_1_2_5_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9610(58)90515-4"},{"key":"e_1_2_5_11_1","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1097-0096(199707)25:6<336::AID-JCU9>3.0.CO;2-D"},{"key":"e_1_2_5_12_1","doi-asserted-by":"publisher","DOI":"10.4103\/0971-6866.29856"},{"key":"e_1_2_5_13_1","first-page":"126","article-title":"The clinical importance of pericentric inversion of chromosome 9 in prenatal diagnosis","volume":"7","author":"Ait\u2010Allah AS","year":"1997","journal-title":"J Matern Fetal Invest"},{"key":"e_1_2_5_14_1","doi-asserted-by":"publisher","DOI":"10.3349\/ymj.2010.51.5.775"},{"key":"e_1_2_5_15_1","first-page":"385","article-title":"A rare seen case with homozygosity for pericentric inversion of chromosome 9 and primary infertility","volume":"9","author":"Ceylan G","year":"2008","journal-title":"Am J Case Rep"}],"container-title":["Journal of Obstetrics and Gynaecology Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fjog.12603","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fjog.12603","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/jog.12603","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,24]],"date-time":"2023-09-24T08:57:46Z","timestamp":1695545866000},"score":1,"resource":{"primary":{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/10.1111\/jog.12603"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,12,10]]},"references-count":14,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2015,4]]}},"alternative-id":["10.1111\/jog.12603"],"URL":"https:\/\/doi.org\/10.1111\/jog.12603","archive":["Portico"],"relation":{},"ISSN":["1341-8076","1447-0756"],"issn-type":[{"value":"1341-8076","type":"print"},{"value":"1447-0756","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,12,10]]}}}