Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Browse

Explore conditions, clinical trials, and the organisations running them.

← All categories

Up to: Ectodermal dysplasia syndrome · Inherited renal tubular disease · Syndromic craniosynostosis · Craniosynostosis syndrome, autosomal recessive · Short rib-polydactyly syndrome

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).

0 trials tagged with this condition →