Craniosynostosis-anal anomalies-porokeratosis syndrome

MONDO:0011287

Craniosynostosis - anal anomalies - porokeratosis, 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, craniosynostosis and clavicular hypoplasia, delayed closure of the fontanel, anal anomalies and genitourinary malformations, craniosynostosis, anal anomalies, and porokeratosis

1 clinical trial for this condition and its sub-types, 0 tagged with Craniosynostosis-anal anomalies-porokeratosis syndrome itself.

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Where it sits in the disease tree

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↑ Syndromic craniosynostosis (22)

Including sub-types (1) Tagged with Craniosynostosis-anal anomalies-porokeratosis syndrome (0)

Trials to join now! 1

Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders

Disease control Recruiting now

This early-stage study aims to develop a personalized treatment for children with syndromic craniosynostosis, a group of rare genetic disorders where skull bones fuse too early. The approach uses a nano-engineered gel to deliver custom genetic medicine directly to the affected ar…

Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS • Aim: Disease control

Last updated Sep 10, 2026 00:00 UTC

Craniosynostosis-anal anomalies-porokeratosis syndrome

Where it sits in the disease tree

Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders