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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

36 clinical trials for this condition and its sub-types.

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Sub-types

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

Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Bone disorder (47) Syndromic disease (24) Human disease (14) Craniosynostosis (13) Skeletal system disorder (4) Bone development disease (2) Disease of genetic or genomic mechanism (2)

Trials to join now! 17 Not yet recruiting 7 Not yet finished but already full! 4 Completed 7 Terminated 1

Scientists gather leftover surgical tissue to unlock secrets of bone disease

Knowledge-focused Terminated

This study collected bone, cartilage, skin, and fat tissue from 50 patients undergoing surgery at Children's National Medical Center. The goal was to grow cells from these tissues in the lab and analyze them to better understand bone and connective tissue diseases. The study was …

Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

Last updated Jun 27, 2026 07:52 UTC