{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,17]],"date-time":"2026-04-17T21:51:31Z","timestamp":1776462691027,"version":"3.51.2"},"reference-count":18,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2018,6,20]]},"abstract":"<jats:p>Apert syndrome is a rare congenital disorder characterised by craniosynostosis, midface hypoplasia and syndactyly of hands and feet. Here we present a case of a 44-year-old woman, with a genetic diagnosis of Apert syndrome from birth, who presented with symptomatic left-sided hip osteoarthritis secondary to femoral abnormalities. She proceeded to have a total hip replacement. This case report describes the rare occurrence to identify a possible association between Apert syndrome and hip abnormalities.<\/jats:p>","DOI":"10.1136\/bcr-2017-221789","type":"journal-article","created":{"date-parts":[[2018,7,4]],"date-time":"2018-07-04T06:35:10Z","timestamp":1530686110000},"page":"bcr-2017-221789","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":2,"title":["Apert syndrome: Be aware of the \u2018dodgy\u2019 hip!"],"prefix":"10.1136","volume":"2018","author":[{"given":"Shehzaad Aziz","family":"Khan","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Thomas Steven","family":"Moores","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Charles","family":"Docker","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2018,7,3]]},"reference":[{"key":"2025042705255175000_2018.jul03_1.bcr-2017-221789.1","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1111\/j.1525-1470.2007.00372.x","article-title":"What syndrome is this? 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Unrecognized childhood hip disease: a major cause of idiopathic osteoarthritis of the hip. Louis (M): CV Mosby: In: Proceedings of the Third Open Scientific Meeting of the Hip Society. St, 1975:212\u201328."},{"key":"2025042705255175000_2018.jul03_1.bcr-2017-221789.11","unstructured":"Robin NH , Marni J , Haldeman-Englert CR . FGFR-related craniosynostosis syndromes. Gene Reviews (Internet). 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