학술논문

Rare bilateral presentation of morning glory disc anomaly.
Document Type
Academic Journal
Author
Dedhia CJ; Smt. Kanuri Santhamma centre for Vitreo-Retinal diseases, LV Prasad Eye Institute, Hyderabad, Telangana, India.; Gogri PY; Department of Cornea and Anterior Segment, LV Prasad Eye Institute, Hyderabad, Telangana, India.; Rani PK; LV Prasad Eye Institute, Hyderabad, Telangana, India.
Source
Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 101526291 Publication Model: Electronic Cited Medium: Internet ISSN: 1757-790X (Electronic) Linking ISSN: 1757790X NLM ISO Abbreviation: BMJ Case Rep Subsets: MEDLINE
Subject
Language
English
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.)