{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,30]],"date-time":"2026-04-30T19:50:50Z","timestamp":1777578650483,"version":"3.51.4"},"reference-count":7,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2010,1,1]],"date-time":"2010-01-01T00:00:00Z","timestamp":1262304000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["European Journal of Ophthalmology"],"published-print":{"date-parts":[[2010,1]]},"abstract":"<jats:sec>\n                    <jats:title>Purpose<\/jats:title>\n                    <jats:p>Vitreoretinal dysplasia is characterized by a congenital bilateral nonattachment of the retina. In some cases, anteroposition of the iris and lens can lead to corneolenticular contact and corneal opacity, masquerading as Peters\u2019 anomaly. We report 3 cases of vitreoretinal dysplasia initially diagnosed as Peters\u2019 anomaly.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Case report.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Case 1: In a 3-year-old boy with bilateral corneal opacities, high frequency ultrasound showed iridolenticular adherences as in Peters\u2019 anomaly, but color Doppler imaging of the posterior pole revealed a bilateral total retinal detachment. Case 2: In an 18-month-old boy with bilateral corneal opacity and dense cataract, ultrasound revealed a shallow anterior chamber and bilateral vitreous hemorrhage with retinal detachment. Case 3: In a 6-month-old girl with bilateral central corneal opacity, shallow anterior chamber, iridocorneal synechiae, and a cataract, ultrasound revealed a total retinal detachment in the right eye, and was uncertain in the left eye. Corneal transplantation was attempted in the left eye, but a retinal detachment was discovered peroperatively There were associated central nervous system anomalies.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Vitreoretinal dysplasia is a potentially evolving disease and can lead to anterior chamber thinning, corneal opacity, and secondary glaucoma. Anterior and posterior segment ultrasound is essential to fix the correct diagnosis and prognosis.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/112067211002000134","type":"journal-article","created":{"date-parts":[[2018,1,24]],"date-time":"2018-01-24T11:08:25Z","timestamp":1516792105000},"page":"228-230","source":"Crossref","is-referenced-by-count":6,"title":["Vitreoretinal Dysplasia Masquerading as Peters\u2019 Anomaly"],"prefix":"10.1177","volume":"20","author":[{"given":"Virginie","family":"Martinet","sequence":"first","affiliation":[{"name":"Paediatric Ophthalmology Department, Fondation Ophtalmologique Adolphe de Rothschild, Paris - France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pascal","family":"Dureau","sequence":"additional","affiliation":[{"name":"Paediatric Ophthalmology Department, Fondation Ophtalmologique Adolphe de Rothschild, Paris - France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Olivier","family":"Berg\u00e8s","sequence":"additional","affiliation":[{"name":"Paediatric Ophthalmology Department, Fondation Ophtalmologique Adolphe de Rothschild, Paris - France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Georges","family":"Caputo","sequence":"additional","affiliation":[{"name":"Paediatric Ophthalmology Department, Fondation Ophtalmologique Adolphe de Rothschild, Paris - France"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2018,1,24]]},"reference":[{"key":"bibr1-112067211002000134","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9394(50)90695-7"},{"key":"bibr2-112067211002000134","doi-asserted-by":"publisher","DOI":"10.1136\/bjo.65.9.631"},{"key":"bibr3-112067211002000134","doi-asserted-by":"publisher","DOI":"10.3928\/0191-3913-19850901-03"},{"key":"bibr4-112067211002000134","doi-asserted-by":"publisher","DOI":"10.1016\/S0002-9394(14)70899-2"},{"key":"bibr5-112067211002000134","doi-asserted-by":"publisher","DOI":"10.1038\/sj.eye.6702840"},{"key":"bibr6-112067211002000134","doi-asserted-by":"publisher","DOI":"10.1136\/bjo.86.1.62"},{"key":"bibr7-112067211002000134","doi-asserted-by":"publisher","DOI":"10.1016\/0039-6257(75)90034-X"}],"container-title":["European Journal of Ophthalmology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/112067211002000134","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/112067211002000134","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,28]],"date-time":"2026-04-28T19:35:06Z","timestamp":1777404906000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/112067211002000134"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,1]]},"references-count":7,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2010,1]]}},"alternative-id":["10.1177\/112067211002000134"],"URL":"https:\/\/doi.org\/10.1177\/112067211002000134","relation":{},"ISSN":["1120-6721","1724-6016"],"issn-type":[{"value":"1120-6721","type":"print"},{"value":"1724-6016","type":"electronic"}],"subject":[],"published":{"date-parts":[[2010,1]]}}}