Craniosynostosis - anal anomalies - porokeratosis (Orphanet_85199), or CDAGS, is a very rare condition characterized by craniosynostosis and clavicular hypoplasia, (C), delayed closure of the fontanel (D), anal anomalies (A), genitourinary malformations (G) and skin eruption (S). Also known as: CAP syndrome, CDAGS syndrome.