Ritscher-Schinzel syndrome

MONDO:0019078

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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary neurological disease (5772) ↑ Congenital nervous system disorder (284) ↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ Central nervous system malformation (51)

Sub-types of Ritscher-Schinzel syndrome

Including sub-types (1) Tagged with Ritscher-Schinzel syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.