{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,9]],"date-time":"2026-06-09T18:23:20Z","timestamp":1781029400834,"version":"3.54.1"},"reference-count":30,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2019,8,2]],"date-time":"2019-08-02T00:00:00Z","timestamp":1564704000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Exper Ophthalmology"],"published-print":{"date-parts":[[2019,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Importance<\/jats:title><jats:p>To determine visual and surgical results in children with Marfan syndrome.<\/jats:p><\/jats:sec><jats:sec><jats:title>Background<\/jats:title><jats:p>Marfan syndrome involves ocular complications which can lead to visual disturbance and amblyopia. Data about the visual and surgical results in children with Marfan syndrome is vital for the clinical management of these patients.<\/jats:p><\/jats:sec><jats:sec><jats:title>Design<\/jats:title><jats:p>Retrospective data analysis.<\/jats:p><\/jats:sec><jats:sec><jats:title>Participants<\/jats:title><jats:p>Eighty\u2010two eyes of 41 patients with a genetically proved diagnosis of Marfan syndrome.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Medical records of patients with Marfan syndrome were reviewed between 2007 and 2017. Ocular complications, visual acuity (VA) of patients with\/without lensectomy and surgical method were evaluated.<\/jats:p><\/jats:sec><jats:sec><jats:title>Main Outcome Measures<\/jats:title><jats:p>VA outcomes of patients with Marfan syndrome with\/without surgical repair of ectopia lentis.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>In 27 (66%) of the 41 patients a bilateral subluxation of the lens was visible and 14 (52%) patients received lensectomy. The mean age at initial presentation was 12.3\u2009\u00b1\u20099\u2009years and mean follow\u2010up was 3\u2009years (range 1\u20107). VA varied from 1.2 to \u22120.1 logMAR at first examination. At initial presentation, mean VA was 0.1\u2009\u00b1\u20090.7 logMAR in patients with a normal lens status (n = 14) and 0.3\u2009\u00b1\u20090.5 logMAR in patients with subluxation of the lens (n = 27) (<jats:italic>P<\/jats:italic>\u2009&lt;\u2009.01). VA improved from 0.2\u2009\u00b1\u20090.5 logMAR to 0.1\u2009\u00b1\u20090.5 logMAR (<jats:italic>P<\/jats:italic> = .06) in children with subluxation of the lens who did not need a lensectomy (n = 12) and from 0.5\u2009\u00b1\u20090.5 logMAR to 0.2\u2009\u00b1\u20090.5 logMAR (<jats:italic>P<\/jats:italic> = .02) in patients who were referred to lensectomy with\/without secondary lens implantation.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions and Relevance<\/jats:title><jats:p>In Marfan syndrome subluxation of the lens was found in the majority of children. Improvement of VA resulted in children with subluxation of the lens and following lensectomy.<\/jats:p><\/jats:sec>","DOI":"10.1111\/ceo.13596","type":"journal-article","created":{"date-parts":[[2019,7,20]],"date-time":"2019-07-20T04:48:30Z","timestamp":1563598110000},"page":"1138-1145","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":24,"title":["Visual outcome and surgical results in children with Marfan syndrome"],"prefix":"10.1111","volume":"47","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3153-7129","authenticated-orcid":false,"given":"Sandra","family":"Rezar\u2010Dreindl","sequence":"first","affiliation":[{"name":"Department of Ophthalmology and Optometry Medical University of Vienna  Vienna Austria"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eva","family":"Stifter","sequence":"additional","affiliation":[{"name":"Department of Ophthalmology and Optometry Medical University of Vienna  Vienna Austria"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas","family":"Neumayer","sequence":"additional","affiliation":[{"name":"Department of Ophthalmology and Optometry Medical University of Vienna  Vienna Austria"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrea","family":"Papp","sequence":"additional","affiliation":[{"name":"Department of Ophthalmology and Optometry Medical University of Vienna  Vienna Austria"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andreas","family":"Gschliesser","sequence":"additional","affiliation":[{"name":"Department of Ophthalmology and Optometry Medical University of Vienna  Vienna Austria"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ursula","family":"Schmidt\u2010Erfurth","sequence":"additional","affiliation":[{"name":"Department of Ophthalmology and Optometry Medical University of Vienna  Vienna Austria"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2019,8,2]]},"reference":[{"key":"e_1_2_6_2_1","volume-title":"Gene Reviews R","author":"Dietz H","year":"2001"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.gde.2007.04.006"},{"key":"e_1_2_6_4_1","first-page":"2242","article-title":"Is ectopia lentis in some cases a mild phenotypic expression of Marfan syndrome? 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