동공잔유막 1례

Other Titles
An Unusual Case of Persistent Pupillary Membrane
Authors
김상진김광수오준섭
Department
Dept. of Ophthalmology (안과학)
Issue Date
1987
Citation
Keimyung Medical Journal, Vol.6(1) : 149-152, 1987
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.
URI
http://kumel.medlib.dsmc.or.kr/handle/2015.oak/14474
Appears in Collections:
1. Journal Papers (연구논문) > 1. School of Medicine (의과대학) > Dept. of Ophthalmology (안과학)
2. Keimyung Medical Journal (계명의대 학술지) > 1987
Keimyung Author(s)
김상진; 김광수; 오준섭
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