계명대학교 의학도서관 Repository

동공잔유막 1례

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Author(s)
김상진김광수오준섭
Keimyung Author(s)
Kim, Sang JinKim, Kwang SooOh, Joon Sup
Department
Dept. of Ophthalmology (안과학)
Journal Title
Keimyung Medical Journal
Issued Date
1987
Volume
6
Issue
1
Abstract
Persistence of a pupillary membrane is due to incomplete atrophy (resorption) of the fetal vascular arcades and associated mesodermal tissue derived from the primitive annular vessel. It is one of the most common, albeit usually clinically innocuous, congenital malformations of the eye. Corgenital pupillary membranes always arise at the collarette. Total persistence of the pupillary membrane is extremely rare and usually associated with other ocular anomalies, especially microphthalmos. The author describe a 15 year old female patient with amblyopia (0. D.) secondary to an extensive, bilateral persistence of the pupillary membrane unassociated with any other ocular anomaly, who received successful surgical removal.
Alternative Title
An Unusual Case of Persistent Pupillary Membrane
Keimyung Author(s)(Kor)
김상진
김광수
오준섭
Publisher
Keimyung University School of Medicine
Citation
김상진 et al. (1987). 동공잔유막 1례. Keimyung Medical Journal, 6(1), 149–152.
Type
Article
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/14474
Appears in Collections:
2. Keimyung Medical Journal (계명의대 학술지) > 1987
1. School of Medicine (의과대학) > Dept. of Ophthalmology (안과학)
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