Literature DB >> 27571914

Rare bilateral presentation of morning glory disc anomaly.

Chintan Jethalal Dedhia1, Pratik Yeshwant Gogri2, Padmaja Kumari Rani3.   

Abstract

A 4-year-old girl presented with a history of poor vision and oscillation of both eyes since infancy. Ocular examination revealed the best corrected visual acuity of 2/60 in right eye and 3/60 in left eye. Horizontal pendular nystagmus was present in both eyes. Fundus examination revealed morning glory disc anomaly (MGDA) bilaterally. Radiographic imaging of the brain revealed central nervous system anomalies. The guarded visual prognosis was explained and the patient referred for low vision rehabilitation and advised yearly follow-up. MGDA is very rarely bilateral. We aim to highlight the distinguishing features of bilateral MGDA from other excavated optic nerve head anomalies which could also present bilaterally but vary in their associations, management and prognosis. 2016 BMJ Publishing Group Ltd.

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Mesh:

Year:  2016        PMID: 27571914      PMCID: PMC5015147          DOI: 10.1136/bcr-2016-215846

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  15 in total

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Journal:  Eye (Lond)       Date:  2012-01-13       Impact factor: 3.775

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Authors:  Nilanjana Deb; Rita Das; I S Roy
Journal:  Indian J Ophthalmol       Date:  2003-06       Impact factor: 1.848

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Authors:  H S Eustis; M R Sanders; T Zimmerman
Journal:  Arch Ophthalmol       Date:  1994-02

Review 10.  The systemic and genetic significance of congenital optic disc anomalies.

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