{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,7]],"date-time":"2025-11-07T00:15:18Z","timestamp":1762474518247,"version":"build-2065373602"},"reference-count":7,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2017,4,3]],"date-time":"2017-04-03T00:00:00Z","timestamp":1491177600000},"content-version":"vor","delay-in-days":92,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Case Reports in Orthopedics"],"published-print":{"date-parts":[[2017,1]]},"abstract":"<jats:p>Ischiospinal Dysostosis (ISD) is a complex and very rare medical entity. It is associated with kyphoscoliosis, dysplasia or aplasia of the ischial rami, segmental anomalies of the bony vertebrae, and peculiar facial morphologies. In this case report, we present a child with Ischiospinal Dysostosis and Pierre\u2010Robin Syndrome. This case report is unique as we followed the patient for 13 years in which he had multiple spinal procedures to treat his kyphoscoliosis. In this paper, we elucidated the number of case reports with documented follow\u2010up regarding spinal cord injury or other complications of ISD and its management.<\/jats:p>","DOI":"10.1155\/2017\/8263536","type":"journal-article","created":{"date-parts":[[2017,4,3]],"date-time":"2017-04-03T17:26:29Z","timestamp":1491240389000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Ischiospinal Dysostosis in a Child with Pierre\u2010Robin Syndrome"],"prefix":"10.1155","volume":"2017","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5532-0314","authenticated-orcid":false,"given":"Mahmoud","family":"Almasri","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Waleed","family":"Kishta","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8304-3561","authenticated-orcid":false,"given":"Fahad H.","family":"Abduljabbar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vincent","family":"Arlet","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7491-9234","authenticated-orcid":false,"given":"Neil","family":"Saran","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jean","family":"Oullet","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2017,4,3]]},"reference":[{"key":"e_1_2_6_1_2","doi-asserted-by":"publisher","DOI":"10.1007\/s002470050556"},{"key":"e_1_2_6_2_2","first-page":"127","article-title":"Massive spinal-ischial dysplasia and extensive spinal dyssegmentation in a Tunisian child with severe form of Cleido-cranial dysplasia","volume":"8","author":"Al Kaissi A.","year":"2005","journal-title":"African Journal of Biomedical Research"},{"key":"e_1_2_6_3_2","doi-asserted-by":"publisher","DOI":"10.1007\/s002470050574"},{"key":"e_1_2_6_4_2","doi-asserted-by":"publisher","DOI":"10.1097\/00019605-200304000-00005"},{"key":"e_1_2_6_5_2","first-page":"29","article-title":"Ischiopubic hypoplasia: a rare constituent of congentinal syndromes","volume":"69","author":"Sferorpoulos N. 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