Cataract surgery in Knobloch syndrome: a case report
Carmen Sílvia Bongiovanni1, Carla Cristina Serra Ferreira1, Ana Paula Silvério Rodrigues1, João Borges Fortes Filho2, Márcia Beatriz Tartarella11Department of Ophthalmology, Congenital Cataract Section, Medical School, Federal University of...
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Dove Medical Press
2011
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oai:doaj.org-article:994200cb7b0f40cea4f4f349e75501382021-12-02T06:22:17ZCataract surgery in Knobloch syndrome: a case report1177-54671177-5483https://doaj.org/article/994200cb7b0f40cea4f4f349e75501382011-06-01T00:00:00Zhttp://www.dovepress.com/cataract-surgery-in-knobloch-syndrome-a-case-report-a7589https://doaj.org/toc/1177-5467https://doaj.org/toc/1177-5483Carmen Sílvia Bongiovanni1, Carla Cristina Serra Ferreira1, Ana Paula Silvério Rodrigues1, João Borges Fortes Filho2, Márcia Beatriz Tartarella11Department of Ophthalmology, Congenital Cataract Section, Medical School, Federal University of São Paulo, São Paulo; 2Department of Ophthalmology, Medical School, Federal University of Rio Grande do Sul, Porto Alegre, BrazilAbstract: Knobloch syndrome is an autosomal recessive disorder associated with early-onset ocular abnormalities and central nervous system malformations. Ocular abnormalities are usually severe, and include high myopia, vitreoretinal degeneration, retinal detachment, macular abnormalities, and cataract. The most frequent systemic changes are midline malformations of the brain, ventricular dilation, and occipital encephalocele. Cognitive delay may occur. We report a case of cataract in a child with Knobloch syndrome. Cataract surgery and follow-up are described.Keywords: Knobloch syndrome, cataract, phacoemulsification, vitreous, right eye, left eye, geneticBongiovanni CSFerreira CCSRodrigues APSFortes Filho JBTartarella MBDove Medical PressarticleOphthalmologyRE1-994ENClinical Ophthalmology, Vol 2011, Iss default, Pp 735-737 (2011) |
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Ophthalmology RE1-994 Bongiovanni CS Ferreira CCS Rodrigues APS Fortes Filho JB Tartarella MB Cataract surgery in Knobloch syndrome: a case report |
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Carmen Sílvia Bongiovanni1, Carla Cristina Serra Ferreira1, Ana Paula Silvério Rodrigues1, João Borges Fortes Filho2, Márcia Beatriz Tartarella11Department of Ophthalmology, Congenital Cataract Section, Medical School, Federal University of São Paulo, São Paulo; 2Department of Ophthalmology, Medical School, Federal University of Rio Grande do Sul, Porto Alegre, BrazilAbstract: Knobloch syndrome is an autosomal recessive disorder associated with early-onset ocular abnormalities and central nervous system malformations. Ocular abnormalities are usually severe, and include high myopia, vitreoretinal degeneration, retinal detachment, macular abnormalities, and cataract. The most frequent systemic changes are midline malformations of the brain, ventricular dilation, and occipital encephalocele. Cognitive delay may occur. We report a case of cataract in a child with Knobloch syndrome. Cataract surgery and follow-up are described.Keywords: Knobloch syndrome, cataract, phacoemulsification, vitreous, right eye, left eye, genetic |
format |
article |
author |
Bongiovanni CS Ferreira CCS Rodrigues APS Fortes Filho JB Tartarella MB |
author_facet |
Bongiovanni CS Ferreira CCS Rodrigues APS Fortes Filho JB Tartarella MB |
author_sort |
Bongiovanni CS |
title |
Cataract surgery in Knobloch syndrome: a case report |
title_short |
Cataract surgery in Knobloch syndrome: a case report |
title_full |
Cataract surgery in Knobloch syndrome: a case report |
title_fullStr |
Cataract surgery in Knobloch syndrome: a case report |
title_full_unstemmed |
Cataract surgery in Knobloch syndrome: a case report |
title_sort |
cataract surgery in knobloch syndrome: a case report |
publisher |
Dove Medical Press |
publishDate |
2011 |
url |
https://doaj.org/article/994200cb7b0f40cea4f4f349e7550138 |
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1718399951606644736 |