Oculoauricular syndrome

Oculoauricular syndrome, Schorderet type is a rare, genetic developmental defect during embryogenesis characterized by various ophthalmic anomalies (including congenital microphthalmia, microcornea, cataract, anterior segment dysgenesis, ocular coloboma and early onset rod-cone dystrophy), and abnormal external ears (low-set pinna with crumpled helix, narrow intertragic incisure, abnormal bridge connecting the crus of the helix and the anthelix, narrow external acoustic meatus, and lobule aplasia).

Also known as: oculoauricular syndrome, OCACS, Schorderet-Munier-Franceschetti syndrome, microphthalmia, microcornea, anterior segment dysgenesis, cataract, ocular coloboma, retinal pigment epithelium abnormalities, Rod-cone dystrophy, and anomalies of the external Ear, oculoauricular syndrome, Schorderet type

0 clinical trials for this condition and its sub-types, 0 tagged with Oculoauricular syndrome itself.