{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,5]],"date-time":"2025-12-05T12:19:59Z","timestamp":1764937199410},"reference-count":10,"publisher":"SLACK, Inc.","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Ophthalmic Surg Lasers Imaging Retina"],"published-print":{"date-parts":[[2020,8]]},"abstract":"<jats:p>\n            Wagner syndrome is a rare hereditary vitreoretinopathy that has been reported in only about 300 people worldwide. It is caused by a mutation in the\n            <jats:italic>VCAN<\/jats:italic>\n            gene that encodes for the proteoglycan versican, which is a major component of the extracellular matrix of the vitreous gel; retinal detachment is uncommon in these cases. The authors report a case of a 23-year-old male who presented with bilateral combined tractional and rhegmatogenous retinal detachments.\n          <\/jats:p>\n          <jats:p>\n            <jats:bold>\n              [\n              <jats:italic>Ophthalmic Surg Lasers Imaging Retina<\/jats:italic>\n              . 2020;51:467\u2013471.]\n            <\/jats:bold>\n          <\/jats:p>","DOI":"10.3928\/23258160-20200804-07","type":"journal-article","created":{"date-parts":[[2020,8,20]],"date-time":"2020-08-20T16:11:40Z","timestamp":1597939900000},"page":"467-471","source":"Crossref","is-referenced-by-count":7,"title":["Complex Combined Tractional and Rhegmatogenous Retinal Detachment in a Twenty-Three-Year-Old Male With Wagner Syndrome"],"prefix":"10.3928","volume":"51","author":[{"given":"Dhariana","family":"Ac\u00f3n","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rehan M.","family":"Hussain","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nicolas A.","family":"Yannuzzi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Audina M.","family":"Berrocal","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2308","reference":[{"key":"e_1_3_1_2_2","doi-asserted-by":"publisher","DOI":"10.3928\/23258160-20160601-10"},{"key":"e_1_3_1_3_2","first-page":"2040","article-title":"A Family With Wagner Syndrome With Uveitis and a New Versican Mutation","volume":"19","author":"Pierre-Rapha\u00ebl Rothschild","year":"2013","unstructured":"Pierre-Rapha\u00ebl Rothschild, Br\u00e9zin Antoine P, Brigitte Nedelec, Cyril Burin des Roziers, Tiffany Ghiotti, Lucie Orhant. A Family With Wagner Syndrome With Uveitis and a New Versican Mutation. Mol Vis. 2013;19:2040\u20132049. PMID: 24174867","journal-title":"Mol Vis"},{"key":"e_1_3_1_4_2","doi-asserted-by":"publisher","DOI":"10.1136\/bjo.2006.104406"},{"key":"e_1_3_1_5_2","doi-asserted-by":"publisher","DOI":"10.1001\/archophthalmol.2009.273"},{"key":"e_1_3_1_6_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0161-6420(95)30787-7"},{"key":"e_1_3_1_7_2","doi-asserted-by":"publisher","DOI":"10.1001\/archopht.1995.01100050139045"},{"key":"e_1_3_1_8_2","first-page":"759","article-title":"Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes","volume":"19","author":"Tran-Viet KN","year":"2013","unstructured":"Tran-Viet KN, Soler V, Quiette V, et al. Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes. Mol Vis. 2013;19:759\u2013766. PMID:23592912","journal-title":"Mol Vis"},{"key":"e_1_3_1_9_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0039-6257(02)00460-5"},{"key":"e_1_3_1_10_2","doi-asserted-by":"publisher","DOI":"10.1097\/ICB.0000000000000392"},{"key":"e_1_3_1_11_2","doi-asserted-by":"publisher","DOI":"10.3390\/genes9020068"}],"container-title":["Ophthalmic Surgery, Lasers and Imaging Retina"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.healio.com\/doiresolver?doi=10.3928\/23258160-20200804-07","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,2]],"date-time":"2023-05-02T13:54:15Z","timestamp":1683035655000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.healio.com\/doi\/10.3928\/23258160-20200804-07"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,8]]},"references-count":10,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2020,8]]}},"alternative-id":["10.3928\/23258160-20200804-07"],"URL":"https:\/\/doi.org\/10.3928\/23258160-20200804-07","relation":{},"ISSN":["2325-8160","2325-8179"],"issn-type":[{"value":"2325-8160","type":"print"},{"value":"2325-8179","type":"electronic"}],"subject":[],"published":{"date-parts":[[2020,8]]}}}