Craniosynostosis-anal anomalies-porokeratosis syndrome

Get in touch with RARE Concierge.

Contact RARE Concierge

Craniosynostosis-anal anomalies-porokeratosis syndrome

Synonyms: CAP syndrome | CDAGS syndrome

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).

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version April 2024

Newly diagnosed with
Craniosynostosis-anal anomalies-porokeratosis syndrome?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

Clinical Trials

For a list of clinical trials in this disease area, please click here.