Muenke syndrome
MONDO:0011274Muenke syndrome is a syndromic craniosynostosis with significant phenotypic variability, usually characterized by coronal synostosis, midfacial retrusion, strabismus, hearing loss and developmental delay.
Also known as: FGFR3-related craniosynostosis, MNKES, Muenke syndrome, craniosynostosis - dysmorphism - brachydactyly, craniosynostosis brachydactyly, craniosynostosis with facial dysmorphism and brachydactyly syndrome, craniosynostosis-dysmorphism-brachydactyly syndrome, glass-chapman-hockley syndrome
2 clinical trials for this condition and its sub-types, 2 tagged with Muenke syndrome itself.
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Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders
Disease control Recruiting nowThis 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
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Massive database aims to unlock secrets of facial birth defects
Knowledge-focused Recruiting nowThis study is creating a large database of genetic and physical information from 3100 children with craniofacial abnormalities, such as craniosynostosis and Pierre Robin sequence. Researchers will analyze this data to understand why these conditions vary so much from person to pe…
Sponsor: Imagine Institute • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:07 UTC