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Clinical Ophthalmology Volume 5, 2011 - Issue
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Case Report

Cataract surgery in Knobloch syndrome: a case report

Carmen Sílvia Bongiovanni1 Department of Ophthalmology, Congenital Cataract Section, Medical School, Federal University of São Paulo, São Paulo
,
Carla Cristina Serra Ferreira1 Department of Ophthalmology, Congenital Cataract Section, Medical School, Federal University of São Paulo, São Paulo
,
Ana Paula Silvério Rodrigues1 Department of Ophthalmology, Congenital Cataract Section, Medical School, Federal University of São Paulo, São Paulo
,
João Borges Fortes Filho2 Department of Ophthalmology, Medical School, Federal University of Rio Grande do Sul, Porto Alegre, Brazil
&
Márcia Beatriz Tartarella1 Department of Ophthalmology, Congenital Cataract Section, Medical School, Federal University of São Paulo, São PauloCorrespondence[email protected]
Pages 735-737 | Published online: 02 Jun 2011

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Sruthi Arepalli, Meghan M. DeBenedictis, Alex Yuan & Elias I. Traboulsi. (2022) Severe retinal complications in Knobloch Syndrome - Three siblings without clinically apparent occipital defects and a review of the literature. Ophthalmic Genetics 43:3, pages 362-370.
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I Irene Díez García-Prieto, Sara Lopez-Martín, Jacobo Albert, Mar Jiménez de la Peña, Daniel Martín Fernández-Mayoralas, Beatriz Calleja-Pérez, María Teresa Gómez Fernández, Sara Álvarez, Taina Pihlajaniemi, Valerio Izzi & Alberto Fernández-Jaén. (2022) Mutations in the COL18A1 gen associated with knobloch syndrome and structural brain anomalies: a novel case report and literature review of neuroimaging findings. Neurocase 28:1, pages 11-18.
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Amani AlBakri, Nicola G. Ghazi & Arif O. Khan. (2017) Biometry, optical coherence tomography, and further clinical observations in Knobloch syndrome. Ophthalmic Genetics 38:2, pages 138-142.
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