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  Vol. 103 No. 11, November 1985 TABLE OF CONTENTS
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Idiopathic Corneal Endotheliopathy

A Report of Two Cases

Yuichi Ohashi, MD; Shigeru Kinoshita, MD; Tomiya Mano, MD; Akira Kiritoshi, MD; Masato Ohji, MD

Arch Ophthalmol. 1985;103(11):1666-1668.


Abstract

• Two male patients had corneal endotheliopathy of unknown origin. In both patients it was characterized by continuously progressing bullous keratopathy preceded by a line of keratic precipitates resembling a rejection line. The disease was progressive and did not respond to intensive corticosteroid therapy. No virus could be isolated from the aqueous humor, and the aqueous-antibody titers to herpes simplex, varicella zoster, and measles viruses were below detection level.



Author Affiliations

From the Department of Ophthalmology, Osaka (Japan) University Medical School.


Footnotes

Accepted for publication June 28, 1985.

Reprint requests to Department of Ophthalmology, Osaka University Medical School, 1-1-50 Fukushima, Fukushima-ku, Osaka 553, Japan (Dr Ohashi).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Experimental Corneal Endotheliitis in Rabbit
Zheng et al.
IOVS 2000;41:377-385.
ABSTRACT | FULL TEXT  

Congenital Idiopathic Corneal Endotheliopathy
Scott et al.
Arch Ophthalmol 1989;107:1186-1192.
ABSTRACT  

Desquamating Endotheliopathy: An Incipient Iridocorneal Endothelial Syndrome?
Stock et al.
Arch Ophthalmol 1987;105:1378-1381.
ABSTRACT  





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