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CDAGS SYNDROME

Known as: CAP SYNDROME, CRANIOSYNOSTOSIS, ANAL ANOMALIES, AND POROKERATOSIS 
National Institutes of Health

Related topics

Related topics

18 relations

Broader (4)

Anal canalCongenital digestive system anomaliesCraniosynostosisPorokeratosis
Anus, ImperforateAutosomal recessive inheritanceBlepharoptosisBrachycephaly

Papers overview

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2005
2005
Candidate gene analysis in 4 families with CDAGS syndrome (craniosynostosis, delayed fontanel closure and cranial defects, anal and genital anomalies and skin eruption) mapping to chromosome 22q
1979
1979
Child resistant cap syndrome.