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Trigonocephaly 1

MONDO:0008603

Any isolated trigonocephaly in which the cause of the disease is a mutation in the FGFR1 gene.

Also known as: FGFR1 isolated trigonocephaly, isolated trigonocephaly caused by mutation in FGFR1, trigonocephaly 1, trigonocephaly type 1, TRIGNO1, craniosynostosis, metopic

35 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) Human disease (14) Craniosynostosis (13) Skeletal system disorder (4) Bone development disease (2) Disease of genetic or genomic mechanism (2) Isolated craniosynostosis (1)

Trials to join now! 17 Not yet recruiting 6 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