Craniosynostosis-anal anomalies-porokeratosis syndrome

What is Craniosynostosis-anal anomalies-porokeratosis 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).

Other condition names

  • CAP syndrome
  • CDAGS syndrome

Inheritance type

Autosomal recessive


  • Worldwide: <1 in 1,000 000

Age of Onset

  • Infancy
  • Neonatal
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