{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T14:22:04Z","timestamp":1787840524169,"version":"build-2784847793"},"reference-count":7,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","license":[{"start":{"date-parts":[[2025,1,1]],"date-time":"2025-01-01T00:00:00Z","timestamp":1735689600000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2025,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    To describe the management of post-traumatic Descemet\u2019s membrane detachment and intraoperative corneal rupture in a known case of Ehlers-Danlos Syndrome (EDS). A 7-year-old child, a known case of EDS, presented with Descemet\u2019s membrane tear in the right eye for which intracameral sulfur hexafluoride (SF\n                    <jats:sub>6<\/jats:sub>\n                    ) and descemetopexy were done. Intraoperative spontaneous rupture of the cornea was noted during descemetopexy which was managed using cyanoacrylate glue and bandage contact lens. We successfully used cyanoacrylate tissue adhesive glue for sealing of corneal rupture suggesting that it can be considered a treatment option for such cases where there is a lack of tissue strength for suturing.\n                  <\/jats:p>","DOI":"10.4103\/ojo.ojo_153_24","type":"journal-article","created":{"date-parts":[[2025,2,25]],"date-time":"2025-02-25T05:00:12Z","timestamp":1740459612000},"page":"58-60","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["The conundrum of post-traumatic corneal rupture in a patient with Ehlers-Danlos syndrome"],"prefix":"10.4103","volume":"18","author":[{"given":"Parul","family":"Jain","sequence":"first","affiliation":[{"name":"Department of Ophthalmology, Guru Nanak Eye Centre, Maulana Azad Medical College, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Isha","family":"Gupta","sequence":"additional","affiliation":[{"name":"Guru Nanak Eye Centre, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Avani","family":"Hariani","sequence":"additional","affiliation":[{"name":"Guru Nanak Eye Centre, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gahan","family":"Reddy","sequence":"additional","affiliation":[{"name":"Guru Nanak Eye Centre, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2025,2,25]]},"reference":[{"key":"R1-20250225","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1111\/j.1399-0004.2012.01858.x","article-title":"The Ehlers-Danlos syndrome, a disorder with many faces","volume":"82","author":"De Paepe","year":"2012","journal-title":"Clin Genet"},{"key":"R2-20250225","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1006\/mgme.2000.3076","article-title":"Mutations in the lysyl hydroxylase 1 gene that result in enzyme deficiency and the clinical phenotype of Ehlers-Danlos syndrome type VI","volume":"71","author":"Yeowell","year":"2000","journal-title":"Mol Genet Metab"},{"key":"R3-20250225","article-title":"Ehlers-Danlos syndrome (EDS)","author":"Dziak","year":"2021","journal-title":"Salem press Encyclopedia of Health"},{"key":"R4-20250225","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1002\/ajmg.c.31552","article-title":"The 2017 international classification of the Ehlers-Danlos syndromes","volume":"175","author":"Malfait","year":"2017","journal-title":"Am J Med Genet C Semin Med Genet"},{"key":"R5-20250225","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1016\/j.ajhg.2011.12.004","article-title":"Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss","volume":"90","author":"Baumann","year":"2012","journal-title":"Am J Hum Genet"},{"key":"R6-20250225","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1186\/1750-1172-6-46","article-title":"Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): Clinical, molecular and biochemical delineation","volume":"6","author":"Rohrbach","year":"2011","journal-title":"Orphanet J Rare Dis"},{"key":"R7-20250225","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1007\/s00431-014-2429-9","article-title":"Kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype","volume":"174","author":"Abdalla","year":"2015","journal-title":"Eur J Pediatr"}],"container-title":["Oman Journal of Ophthalmology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.4103\/ojo.ojo_153_24","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T13:24:26Z","timestamp":1787837066000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/ojo.ojo_153_24"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,1]]},"references-count":7,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2025]]}},"URL":"https:\/\/doi.org\/10.4103\/ojo.ojo_153_24","relation":{},"ISSN":["0974-620X","0974-7842"],"issn-type":[{"value":"0974-620X","type":"print"},{"value":"0974-7842","type":"electronic"}],"subject":[],"published":{"date-parts":[[2025,1]]},"assertion":[{"value":"2024-05-27","name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2025-01-25","name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}}]}}