{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,3,29]],"date-time":"2022-03-29T19:29:50Z","timestamp":1648582190764},"reference-count":6,"publisher":"Hindawi Limited","license":[{"start":{"date-parts":[[2011,1,1]],"date-time":"2011-01-01T00:00:00Z","timestamp":1293840000000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/3.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Ophthalmological Medicine"],"published-print":{"date-parts":[[2011]]},"abstract":"<jats:p><jats:italic>Purpose<\/jats:italic>. We herein report a patient with bilateral congenital total iris sphincter agenesis with no other abnormality detected on systemic examination.<jats:italic>Methods<\/jats:italic>. A 24-year-old laborer presented to us for a routine checkup with complaint of photophobia and inability to work under sunlight. Examination revealed bilateral absence of sphincter and 6.5\u2009mm pupil in both eyes in the undilated state.<jats:italic>Results<\/jats:italic>. Accommodation was poor in both eyes. Systemic examination was within normal limits. He was prescribed bifocal photochromic glasses for constant wear.<jats:italic>Conclusions<\/jats:italic>. Congenital sphincter agenesis can occur in an isolated form without systemic abnormalities which can be managed conservatively.<\/jats:p>","DOI":"10.1155\/2011\/479092","type":"journal-article","created":{"date-parts":[[2011,12,14]],"date-time":"2011-12-14T16:25:49Z","timestamp":1323879949000},"page":"1-2","source":"Crossref","is-referenced-by-count":0,"title":["Isolated Bilateral Congenital Iris Sphincter Agenesis"],"prefix":"10.1155","volume":"2011","author":[{"given":"Aparna","family":"Rao","sequence":"first","affiliation":[{"name":"Glaucoma Services, LV Prasad Eye Institute, Patia, Orissa, Bhubaneswar 751024, India"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"98","reference":[{"key":"1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1600-0420.2005.00496.x"},{"issue":"4","key":"2","first-page":"509","volume":"120","year":"2002","journal-title":"Archives of Ophthalmology"},{"issue":"3","key":"3","first-page":"318","volume":"131","year":"2004","journal-title":"American Journal of Medical Genetics A"},{"issue":"4","key":"4","doi-asserted-by":"crossref","first-page":"515","DOI":"10.1016\/0002-9394(76)90312-3","volume":"81","year":"1976","journal-title":"American Journal of Ophthalmology"},{"issue":"4","key":"5","first-page":"377","volume":"93","year":"1996","journal-title":"Ophthalmologe"},{"issue":"2","key":"6","first-page":"72","volume":"28","year":"1993","journal-title":"Canadian Journal of Ophthalmology"}],"container-title":["Case Reports in Ophthalmological Medicine"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/downloads.hindawi.com\/journals\/criopm\/2011\/479092.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/downloads.hindawi.com\/journals\/criopm\/2011\/479092.xml","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/downloads.hindawi.com\/journals\/criopm\/2011\/479092.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,6,20]],"date-time":"2017-06-20T07:21:32Z","timestamp":1497943292000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.hindawi.com\/journals\/criopm\/2011\/479092\/"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011]]},"references-count":6,"alternative-id":["479092","479092"],"URL":"https:\/\/doi.org\/10.1155\/2011\/479092","relation":{},"ISSN":["2090-6722","2090-6730"],"issn-type":[{"value":"2090-6722","type":"print"},{"value":"2090-6730","type":"electronic"}],"subject":[],"published":{"date-parts":[[2011]]}}}