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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.

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Sub-types

Bazopoulou Kyrkanidou syndrome (0) Cote katsantoni syndrome (0)

Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Syndromic disease (25) Craniosynostosis (15) Human disease (14) Skeletal system disorder (4) Bone development disease (2) Disease of genetic or genomic mechanism (2)

Not yet recruiting 1

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

Disease control Not yet recruiting

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 Jun 27, 2026 12:09 UTC