Double temporal retinochoroidal coloboma with posterior embyotoxon and persistent pupillary membrane: a case report.
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus(2024)
摘要
Ocular colobomas are typically located in the inferonasal quadrant and attributable to defective fetal fissure closure. Colobomas can, however, affect any part of the eye, from the eyelid to the optic nerve. We present the case of a 7-year-old girl with two retinochoroidal colobomas in an atypical temporal location, with associated other ocular defects.
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