| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4031104 | Ophthalmology | 2006 | 8 Pages |
Abstract
Fuchs' syndrome in Chinese patients is characterized by a mild uveitis with characteristic KPs, varying degrees of iris depigmentation, and, occasionally, heterochromia. Exudates adjacent to the ciliary body and subclinical retinal and optic nerve involvement were common in the patients who were studied by UBM and FFA.
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Authors
Peizeng MD, PhD, Wang MD, Haoli PhD, Bing PhD, Xuan PhD, Aize PhD,