Craniosynostosis-anal anomalies-porokeratosis syndrome
MONDO:0011287Craniosynostosis - 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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