Muenke syndrome is a syndromic craniosynostosis with significant phenotypic variability usually characterized by coronal synostosis midfacial retrusion strabismus hearing loss and developmental delay.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version March 2024
Newly diagnosed with
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