TCF12-related craniosynostosis

MONDO:0014128

Any syndromic craniosynostosis in which the cause of the disease is a mutation in the TCF12 gene.

Also known as: TCF12 craniosynostosis, TCF12-related craniosynostosis, craniosynostosis 3, craniosynostosis caused by mutation in TCF12, craniosynostosis type 3, CRS3

1 clinical trial for this condition and its sub-types, 0 tagged with TCF12-related craniosynostosis itself.

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Where it sits in the disease tree

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↑ Syndromic craniosynostosis (22)

Including sub-types (1) Tagged with TCF12-related craniosynostosis (0)

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

TCF12-related craniosynostosis

Where it sits in the disease tree

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