Cure My Disease

Don't miss your cure!

Log in / Sign up

TWIST1-related craniosynostosis

MONDO:0007399

Any craniosynostosis in which the cause of the disease is a mutation in the TWIST1 gene.

Also known as: Primary Craniosynostosis, TWIST1-related craniosynostosis, craniosynostosis 1, craniosynostosis type 1, CRS, CRS1, craniostenosis

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

Follow this condition to get notified about new trials

Broader categories

Disease (717) Musculoskeletal system disorder (214) Hereditary disease (188) Bone disorder (51) Craniosynostosis (16) Human disease (15) Skeletal system disorder (4) Bone development disease (2) Disease of genetic or genomic mechanism (2) Isolated craniosynostosis (1)

Not yet recruiting 1 Not yet finished but already full! 1

Infant skull study aims to unlock secrets of craniosynostosis

Knowledge-focused Not yet recruiting

This study looks at skull bone samples from 80 infants aged 3 to 12 months who have craniosynostosis, a condition where skull bones fuse too early. Researchers will measure the bone's strength, structure, and tissue makeup both near and far from the fused area. The goal is to bet…

Sponsor: Hospices Civils de Lyon • Aim: Knowledge-focused

Last updated Jun 27, 2026 14:00 UTC