{Reference Type}: Case Reports
{Title}: Double temporal retinochoroidal coloboma with posterior embyotoxon and persistent pupillary membrane: a case report.
{Author}: Dhillon HK;Narote KD;Agarkar S;
{Journal}: J AAPOS
{Volume}: 28
{Issue}: 1
{Year}: 2024 02 18
{Factor}: 1.325
{DOI}: 10.1016/j.jaapos.2023.11.018
{Abstract}: 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.