Craniosynostosis–anal anomalies–porokeratosis syndrome

Craniosynostosis–anal anomalies–porokeratosis syndrome
Classification and external resources
OMIM 603116

Craniosynostosis–anal anomalies–porokeratosis syndrome (also known as "CAP syndrome") is a cutaneous condition inherited in an autosomal recessive fashion.[1]

See also

References

  1. ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.


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