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Up to: Hereditary neurological disease · Congenital nervous system disorder · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Central nervous system malformation
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.
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Ritscher-Schinzel syndrome 1 0 trials
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Ritscher-Schinzel syndrome 2 0 trials
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Ritscher-Schinzel syndrome 3 0 trials
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Ritscher-Schinzel syndrome 4 0 trials