Crouzon syndrome

MONDO:0007405

Crouzon disease is characterized by craniosynostosis and facial hypoplasia.

Also known as: Crouzon craniofacial dysostosis, Crouzon syndrome, craniofacial dysostosis, Cfd1, Crouzon disease, craniofacial dysostosis type 1, craniofacial dysostosis, type 1

1 clinical trial for this condition and its sub-types, 1 tagged with Crouzon syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Syndromic craniosynostosis (22)

Sub-types of Crouzon syndrome

Bazopoulou Kyrkanidou syndrome 0 trials
Cote katsantoni syndrome 0 trials

Including sub-types (1) Tagged with Crouzon syndrome (1)

Trials to join now! 1

Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders

Disease control Recruiting now

This early-stage study aims to develop a personalized treatment for children with syndromic craniosynostosis, a group of rare genetic disorders where skull bones fuse too early. The approach uses a nano-engineered gel to deliver custom genetic medicine directly to the affected ar…

Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS • Aim: Disease control

Last updated Sep 10, 2026 00:00 UTC

Crouzon syndrome

Where it sits in the disease tree

Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders