{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,14]],"date-time":"2026-04-14T20:28:26Z","timestamp":1776198506592,"version":"3.50.1"},"reference-count":7,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2017,10,1]],"date-time":"2017-10-01T00:00:00Z","timestamp":1506816000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2017,10,1]],"date-time":"2017-10-01T00:00:00Z","timestamp":1506816000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jaapos.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of American Association for Pediatric Ophthalmology and Strabismus"],"published-print":{"date-parts":[[2017,10]]},"DOI":"10.1016\/j.jaapos.2017.04.016","type":"journal-article","created":{"date-parts":[[2017,9,1]],"date-time":"2017-09-01T13:46:40Z","timestamp":1504273600000},"page":"422-425.e1","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":9,"title":["Revesz syndrome masquerading as traumatic retinal detachment"],"prefix":"10.1016","volume":"21","author":[{"given":"Kareem","family":"Moussa","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"James N.","family":"Huang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anthony T.","family":"Moore","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jaapos.2017.04.016_bib1","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1586\/ehm.13.23","article-title":"Updates on the biology and management of dyskeratosis congenita and related telomere biology disorders","volume":"6","author":"Ballew","year":"2013","journal-title":"Expert Rev Hematol"},{"key":"10.1016\/j.jaapos.2017.04.016_bib2","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1136\/jmg.29.9.673","article-title":"Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?","volume":"29","author":"Revesz","year":"1992","journal-title":"J\u00a0Med Genet"},{"key":"10.1016\/j.jaapos.2017.04.016_bib3","doi-asserted-by":"crossref","first-page":"3594","DOI":"10.1182\/blood-2008-05-153445","article-title":"TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes","volume":"112","author":"Walne","year":"2008","journal-title":"Blood"},{"key":"10.1016\/j.jaapos.2017.04.016_bib4","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1080\/13816810.2016.1275019","article-title":"Retinal findings and a novel TINF2 mutation in Revesz syndrome: clinical and molecular correlations with pediatric retinal vasculopathies","volume":"38","author":"Gupta","year":"2017","journal-title":"Ophthalmic Genet"},{"key":"10.1016\/j.jaapos.2017.04.016_bib5","doi-asserted-by":"crossref","first-page":"615","DOI":"10.1016\/j.ophtha.2009.08.023","article-title":"Ocular and orbital manifestations of the inherited bone marrow failure\u00a0syndromes: Fanconi anemia and dyskeratosis congenita","volume":"117","author":"Tsilou","year":"2010","journal-title":"Ophthalmology"},{"key":"10.1016\/j.jaapos.2017.04.016_bib6","doi-asserted-by":"crossref","first-page":"134","DOI":"10.1001\/archophthalmol.2007.4","article-title":"Bilateral retinal vasculopathy in a patient with dyskeratosis congenita","volume":"126","author":"Teixeira","year":"2008","journal-title":"Arch Ophthalmol"},{"key":"10.1016\/j.jaapos.2017.04.016_bib7","doi-asserted-by":"crossref","first-page":"181","DOI":"10.3109\/13816810903148012","article-title":"Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita","volume":"30","author":"Johnson","year":"2009","journal-title":"Ophthalmic Genet"}],"container-title":["Journal of American Association for Pediatric Ophthalmology and Strabismus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1091853116304451?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1091853116304451?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T20:22:03Z","timestamp":1761078123000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1091853116304451"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,10]]},"references-count":7,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2017,10]]}},"alternative-id":["S1091853116304451"],"URL":"https:\/\/doi.org\/10.1016\/j.jaapos.2017.04.016","relation":{},"ISSN":["1091-8531"],"issn-type":[{"value":"1091-8531","type":"print"}],"subject":[],"published":{"date-parts":[[2017,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Revesz syndrome masquerading as traumatic retinal detachment","name":"articletitle","label":"Article Title"},{"value":"Journal of American Association for Pediatric Ophthalmology and Strabismus","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jaapos.2017.04.016","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 American Association for Pediatric Ophthalmology and Strabismus. Published by Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}