{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,15]],"date-time":"2026-01-15T00:58:07Z","timestamp":1768438687192,"version":"3.49.0"},"reference-count":7,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"C","license":[{"start":{"date-parts":[[2020,1,1]],"date-time":"2020-01-01T00:00:00Z","timestamp":1577836800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,1,1]],"date-time":"2020-01-01T00:00:00Z","timestamp":1577836800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2020,9,7]],"date-time":"2020-09-07T00:00:00Z","timestamp":1599436800000},"content-version":"vor","delay-in-days":250,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2020,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Introduction<\/jats:title>\n                    <jats:p>Marfan syndrome (MFS) is a disorder of the connective tissue that is inherited in an autosomal dominant fashion and is caused by mutations in the gene coding for fibrillin-1 (FBN1). This condition commonly affects the skeletal system, pulmonary system, ocular system and the cardiovascular system. Surgical intervention is often needed to correct the various deformities affecting the patients to restore the function, improving the patient\u2019s aesthetic appearance and quality of life.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Presentation of case<\/jats:title>\n                    <jats:p>It\u2019s a rare case report of a young male patient suffering through unilateral temporomandibular joint ankylosis, obstructive sleep apnea and unaesthetic appearance while being a case of Marfan syndrome.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Discussion<\/jats:title>\n                    <jats:p>This paper highlights the various surgical procedures undertaken to correct the deformities affecting the individual and improving the overall health of the patient.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>Our patient\u2019s management shows the necessity of a multidisciplinary, multi factorial and multi-faceted approach with early visual identification and diagnosis.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Highlights<\/jats:title>\n                  <\/jats:sec>","DOI":"10.1016\/j.ijscr.2020.09.033","type":"journal-article","created":{"date-parts":[[2020,9,11]],"date-time":"2020-09-11T11:53:49Z","timestamp":1599825229000},"page":"157-161","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":4,"title":["Management of unilateral temporomandibular joint ankylosis &amp; orthomorphic correction in a patient with Marfan syndrome"],"prefix":"10.1097","volume":"75","author":[{"given":"B. M.","family":"Rudagi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jain","family":"Rishabh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Merchant","family":"Arif","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chourasia","family":"Namrata","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Naikwade","family":"Shahbaaz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bhavar","family":"Gaurav","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R3-36-20260114","doi-asserted-by":"crossref","first-page":"1429","DOI":"10.1002\/ccr3.1058","article-title":"Oral manifestations of a rare variant of Marfan syndrome","volume":"5","author":"Sinha","year":"2017","journal-title":"Clin. Case Rep"},{"key":"R4-36-20260114","doi-asserted-by":"crossref","first-page":"137","DOI":"10.2147\/TACG.S60472","article-title":"Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome","volume":"8","author":"Kodolitsch","year":"2015","journal-title":"Appl. Clin. Genet"},{"key":"R6-36-20260114","doi-asserted-by":"crossref","first-page":"592","DOI":"10.1016\/j.tripleo.2003.10.024","article-title":"Temporomandibular joint dysfunction in Marfan syndrome","volume":"97","author":"Bauss","year":"2004","journal-title":"Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod"},{"key":"R7-36-20260114","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1016\/j.ijporl.2018.06.014","article-title":"Obstructive sleep apnea in children with Marfan syndrome: relationships between three-dimensional palatal morphology and apnea-hypopnea index","volume":"112","author":"Paoloni","year":"2018","journal-title":"Int. J. Pediatr. Otorhinolaryngol"},{"key":"R9-36-20260114","doi-asserted-by":"crossref","first-page":"564","DOI":"10.1067\/moe.2002.121430","article-title":"Oral manifestations of patients with Marfan syndrome: a case-control study","volume":"93","author":"De Coster","year":"2002","journal-title":"Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod"},{"key":"R10-36-20260114","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1016\/S1010-5182(97)80001-7","article-title":"Management of unilateral temporomandibular ankylosis associated with facial asymmetry","volume":"25","author":"El-Sheikh","year":"1997","journal-title":"J. Cranio-Maxillof Acial Surg"},{"key":"R11-36-20260114","doi-asserted-by":"crossref","first-page":"132","DOI":"10.1016\/j.ijsu.2018.10.028","article-title":"The SCARE 2018 statement: updating consensus surgical case report (SCARE) guidelines","volume":"60","author":"Agha","year":"2018","journal-title":"Int. J. Surg"}],"container-title":["International Journal of Surgery Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2210261220307057?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2210261220307057?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.lww.com\/10.1016\/j.ijscr.2020.09.033","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T13:47:51Z","timestamp":1768398471000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/10.1016\/j.ijscr.2020.09.033"}},"subtitle":["A rare case report"],"short-title":[],"issued":{"date-parts":[[2020,1]]},"references-count":7,"journal-issue":{"issue":"C","published-print":{"date-parts":[[2020]]}},"URL":"https:\/\/doi.org\/10.1016\/j.ijscr.2020.09.033","relation":{},"ISSN":["2210-2612"],"issn-type":[{"value":"2210-2612","type":"print"}],"subject":[],"published":{"date-parts":[[2020,1]]}}}