Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/1724
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dc.contributor.authorDarshan Kumar U, Sunil G Biradar.-
dc.date.accessioned2020-01-16T09:40:58Z-
dc.date.available2020-01-16T09:40:58Z-
dc.date.issued2015-03-
dc.identifier.urihttp://hdl.handle.net/123456789/1724-
dc.description.abstractReporting a case of Peters’ type II with congenital heart defect a rare form of anterior segment dysgenesis in which abnormal cleavage of the anterior chamber occurs. It is characterized by central corneal opacification secondary to defects in a posterior corneal stroma, Descemet's membrane, and endothelium. Majority of cases are sporadic, bilateral, and associated with other systemic malformations. MATERIAL AND METHOD: A18 year old female presented with a history of bilateral cloudy corneas and diminution of vision since early childhooden_US
dc.language.isoenen_US
dc.publisherBLDE(Deemed to be University)en_US
dc.subjectpeters’ type II anomaly, anterior segment dysgenesis, microcornea, congenital heart defect. INTRODUCTION: Peters' anomaly is a rare form of anterior segment dysgenesis in whichen_US
dc.titlePater’s type II anomaly associated with congenital heart defect: Rare case report.en_US
dc.typeArticleen_US
Appears in Collections:Faculty of Ophthalmology

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