Pater’s type  II anomaly associated with congenital heart defect: Rare case report.

Darshan Kumar U, Sunil G Biradar.

dc.contributor.author	Darshan Kumar U, Sunil G Biradar.
dc.date.accessioned	2020-01-16T09:40:58Z
dc.date.available	2020-01-16T09:40:58Z
dc.date.issued	2015-03
dc.identifier.uri	http://hdl.handle.net/123456789/1724
dc.description.abstract	Reporting 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 childhood	en_US
dc.language.iso	en	en_US
dc.publisher	BLDE(Deemed to be University)	en_US
dc.subject	peters’ type II anomaly, anterior segment dysgenesis, microcornea, congenital heart defect. INTRODUCTION: Peters' anomaly is a rare form of anterior segment dysgenesis in which	en_US
dc.title	Pater’s type II anomaly associated with congenital heart defect: Rare case report.	en_US
dc.type	Article	en_US