Clinical evaluation of torpedo maculopathy in an infant population with additional genetic testing for NEXMIF mutation.
Gokhan CelikMurat GünayAsli Deger VuralOsman KizilayYasemin Kendir DemirkolMuhammet Kazim ErolPublished in: Eye (London, England) (2021)
Fundoscopic appearance and OCT findings of lesions show similarities to those already reported previously. Contrary to popular belief, a nasally located satellite lesion was observed in one of our case.