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

• Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome
• List of cutaneous conditions

References

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