Literature DB >> 26994503

Infantile-onset glaucoma and anterior megalophthalmos in osteogenesis imperfecta.

Brenda L Bohnsack1.   

Abstract

Osteogenesis imperfecta (OI) is an inherited condition in which defects in type 1 collagen cause abnormalities in many tissues and organs, including bone, teeth, heart valves, and eyes. We describe a 6-month-old boy with OI who presented with anterior megalophthalmos of the right eye and infantile-onset glaucoma of the left eye. To our knowledge, this is the first reported case of these types of congenital eye anomalies in an infant with OI.
Copyright © 2016 American Association for Pediatric Ophthalmology and Strabismus. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 26994503     DOI: 10.1016/j.jaapos.2015.11.005

Source DB:  PubMed          Journal:  J AAPOS        ISSN: 1091-8531            Impact factor:   1.220


  4 in total

1.  Ocular characteristics and complications in patients with osteogenesis imperfecta: a systematic review.

Authors:  Sanne Treurniet; Pia Burger; Ebba A E Ghyczy; Frank D Verbraak; Katie R Curro-Tafili; Dimitra Micha; Nathalie Bravenboer; Stuart H Ralston; Ralph de Vries; Annette C Moll; Elisabeth Marelise W Eekhoff
Journal:  Acta Ophthalmol       Date:  2021-05-19       Impact factor: 3.988

2.  PITX2 deficiency and associated human disease: insights from the zebrafish model.

Authors:  Kathryn E Hendee; Elena A Sorokina; Sanaa S Muheisen; Linda M Reis; Rebecca C Tyler; Vujica Markovic; Goran Cuturilo; Brian A Link; Elena V Semina
Journal:  Hum Mol Genet       Date:  2018-05-15       Impact factor: 6.150

Review 3.  Therapeutic Potential of Mesenchymal Stem Cells and Their Secretome in the Treatment of Glaucoma.

Authors:  C Randall Harrell; Crissy Fellabaum; Aleksandar Arsenijevic; Bojana Simovic Markovic; Valentin Djonov; Vladislav Volarevic
Journal:  Stem Cells Int       Date:  2019-12-27       Impact factor: 5.443

Review 4.  Glaucoma Syndromes: Insights into Glaucoma Genetics and Pathogenesis from Monogenic Syndromic Disorders.

Authors:  Daniel A Balikov; Adam Jacobson; Lev Prasov
Journal:  Genes (Basel)       Date:  2021-09-11       Impact factor: 4.096

  4 in total

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