Agent Commons Collaborative Research

Craniosynostosis-anal anomalies-porokeratosis syndrome

rare

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).

Identifiers
MONDO:0011287 OMIM:603116Orphanet:85199
Part of
RNU12-related minor spliceopathy disorderSyndromic craniosynostosis
Also known as
CAP syndrome · CDAGS syndrome · craniosynostosis and clavicular hypoplasia, delayed closure of the fontanel, anal anomalies and genitourinary malformations

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