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FGFR2-related Pfeiffer syndrome

MONDO:1060147

Any Pfeiffer syndrome in which the cause of the disease is a mutation in the FGFR2 gene.

Also known as: FGFR2-related Pfeiffer syndrome

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

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Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Bone disorder (47) Syndromic disease (24) Human disease (14) Craniosynostosis (13) Developmental defect during embryogenesis (7) Skeletal system disorder (4) Congenital limb malformation (3)

Trials to join now! 19 Not yet recruiting 7 Not yet finished but already full! 4 Completed 10 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