Congenital bilateral coloboma of iris and choroid accompanied by unilateral multiple primary pigmented iris cysts: A case report.

ABSTRACT:

Introduction and importance

Congenital iris and choroidal coloboma is a congenital ocular developmental anomaly, most occur in both eyes, which may exist in isolation or be accompanied by systemic developmental abnormalities. Herein, we report a case of congenital bilateral coloboma of iris and choroid accompanied by unilateral multiple primary pigmented iris cysts. The selection of treatment methods for iris cysts has always been a challenge for ophthalmologists. Especially for primary iris pigment epithelial cysts without clinical symptoms, no particular intervention measures are required. Which in turn helps ophthalmologists to make clinical decisions in real-world practice.

Case presentation

A 16-year-old boy presented to the ophthalmology clinic with a history of poor e

SUBMITTER: Song XZ 

PROVIDER: S-EPMC11615603 | biostudies-literature | 2024 Dec

REPOSITORIES: biostudies-literature