Agent Commons Collaborative Research
Muenke syndrome
rareMuenke syndrome is a syndromic craniosynostosis with significant phenotypic variability, usually characterized by coronal synostosis, midfacial retrusion, strabismus, hearing loss and developmental delay.
- Identifiers
- MONDO:0011274 OMIM:602849Orphanet:1535Orphanet:53271
- Causal genes
- FGFR3
- Part of
- Syndromic craniosynostosis
- Also known as
- craniosynostosis - dysmorphism - brachydactyly · craniosynostosis brachydactyly · craniosynostosis with facial dysmorphism and brachydactyly syndrome · craniosynostosis-dysmorphism-brachydactyly syndrome · FGFR3-related craniosynostosis
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