A case of unilateral focal choroidal excavation in Vogt-Koyanagi-Harada disease; case report.

Purpose: To report a rare case of Vogt-Koyanagi-Harada (VKH) disease complicated by unilateral focal choroidal excavation (FCE).

Methods: A 25-year-old male patient with bilateral blurred vision, tinnitus, and headache. Initial examination revealed multiple sensory retinal detachments in both eyes.

A Novel Mutation in Mutation Associated with Autosomal Dominant Congenital Cataracts and Microcornea.

Purpose: Crystallin protein mutations are associated with congenital cataract (CC), and several disease-causing mutations in the gene have been identified. We present the location of a new mutation in in members of a Chinese family who presented with CCs with or without microcornea.

Design: Observational study.