Craniosynostosis 2

MONDO:0011481

A form of syndromic craniosynostosis, characterized by a highly variable craniosynostosis with frontal bossing, turribrachycephaly and cloverleaf skull anomaly. Hypoplasia of the supraorbital ridges, cleft palate, extra teeth and limb anomalies (triphalangeal thumb, 3-4 syndactyly of the hands, a short first metatarsal, middle phalangeal agenesis in the feet) have also been described. Associated problems include headache, poor vision, and seizures. Intelligence is normal.

Also known as: CRS2, MSX2-related craniosynostosis, Warman-Mulliken-Hayward syndrome, craniosynostosis 2, craniosynostosis type 2, craniosynostosis, Warman type, Warman Mulliken Hayward syndrome, craniosynostosis Warman type

1 clinical trial for this condition and its sub-types, 0 tagged with Craniosynostosis 2 itself.

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