Cranioectodermal dysplasia

Cranioectodermal dysplasia (CED) is a rare developmental disorder characterized by congenital skeletal and ectodermal defects associated with dysmorphic features, nephronophthisis, hepatic fibrosis and ocular anomalies (mainly retinitis pigmentosa).

Also known as: CED, Sensenbrenner syndrome, cranioectodermal dysplasia

59 clinical trials for this condition and its sub-types.