Craniosynostosis, Herrmann-Opitz type

Craniosynostosis, Herrmann-Opitz type is a rare bone development disorder characterized by intellectual disability, short stature, turribrachycephaly, facial dysmorphism (i.e. severe hypertelorism, hypoplasia of supraorbital ridges, abnormal ears, and micrognathia), bony defects of the occiput, and digital anomalies (incl. syndactyly, oligodactyly, and/or brachydactyly). Urethral atresia has also been reported. There have been no further descriptions in the literature since 1987.

Also known as: Herrmann Opitz craniosynostosis

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