Abstract
Chorioretinal coloboma is a rare condition caused by incomplete closure of the embryonic fissure. We report a case of a 34 years old with a unilateral retinal and choroidal coloboma in the right eye, highlighting the use of stereoscopic fundus photograph, spectral-domain optical coherence tomography, and fundus autofluorescence. Regular eye examinations are crucial to detect changes in patients with a higher retinal tear and retinal detachment risk.
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