Ritscher-Schinzel syndrome

Cranio-cerebello-cardiac (3C) syndrome is a rare multiple congenital anomalies syndrome characterized by craniofacial (prominent occiput and forehead, hypertelorism, ocular coloboma, cleft palate), cerebellar (Dandy-Walker malformation, cerebellar vermis hypoplasia) and cardiac (tetralogy of Fallot, atrial and ventricular septal defects) anomalies.

Also known as: 3C syndrome, CCC dysplasia, Craniocerebellocardiac dysplasia, Ritscher-Schinzel syndrome, craniocerebellocardiac dysplasia, Dandy-Walker like malformation with atrioventricular septal defect, Dandy-Walker-like malformation with ASD, Dandy-Walker-like malformation with atrioventricular septal defect

1 clinical trial for this condition and its sub-types, 0 tagged with Ritscher-Schinzel syndrome itself.