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OPHTHALMIC IMAGE |
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Year : 2023 | Volume
: 3
| Issue : 1 | Page : 248 |
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Temporal atypical retinochoroidal coloboma
Gaurav Sanghi, Rajeev Gupta, Anureet Brar
Department of Vitreo-Retina, Sangam Netralaya, Mohali, Punjab, India
Date of Web Publication | 20-Jan-2023 |
Correspondence Address: Gaurav Sanghi Sangam Netralaya, SCO 669, Sector 70, Mohali, Punjab - 160 071 India
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/ijo.IJO_1275_22
How to cite this article: Sanghi G, Gupta R, Brar A. Temporal atypical retinochoroidal coloboma. Indian J Ophthalmol Case Rep 2023;3:248 |
A 4-year-old female presented to us with inward deviation of the left eye since infancy. Anterior segment examination was normal in both eyes. Fundus of the right eye was normal. Indirect ophthalmoscopy of the left eye revealed narrowing of temporal arcade and temporal retinochoroidal coloboma [Figure 1]. The foveal area was involved in the coloboma. | Figure 1: Fundus image of the left eye shows narrowing of vascular arcade and temporal retinochoroidal coloboma
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Very few cases of temporal retinochoroidal coloboma have been reported.[1],[2],[3] Typical inferonasal retinochoroidal coloboma occurs due to defective closure of embryonic fissure.[4] However, atypical colobomas are speculated to occur due to presence of accessory embryonic fissures, rotation of embryonic fissure, and developmental anomalies of neural ectoderm.[3],[5] It is important to recognize this rare entity.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References | |  |
1. | Gupta S, Sethi HS, Naik M. Temporal iridofundal coloboma with persistent pupillary membranes with persistent fetal vasculature. Indian J Ophthalmol 2020;68:1649-50.  [ PUBMED] [Full text] |
2. | Azad S, Mittal K. Atypical choroidal coloboma. Ophthalmol Retina 2018;2:1142. |
3. | Gulati M, Panchal B, Pathengay A. A rare case of temporal atypical retinochoroidal coloboma associated with posterior embryotoxon. Indian J Ophthalmol 2020;68:1445-6.  [ PUBMED] [Full text] |
4. | Onwochei BC, Simon JW, Bateman JB, Couture KC, Mir E. Ocular colobomata. Surv Ophthalmol 2000;45:175-94. |
5. | Hocking JC, Famulski JK, Yoon KH, Widen SA, Bernstein CS, Koch S, et al.; FORGE Canada Consortium. Morphogenetic defects underlie Superior Coloboma, a newly identified closure disorder of the dorsal eye. PLoS Genet 2018;14:e1007246. |
[Figure 1]
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