What is another word for muenke syndrome?
Pronunciation: [mjˈuːəŋk sˈɪndɹə͡ʊm] (IPA) 
Muenke syndrome is a genetic disorder that affects the development of the skull and face. It is also known as FGFR3-related craniosynostosis, Muenke craniosynostosis, or coronal craniosynostosis. The condition occurs when the child is born with an abnormality in the FGFR3 gene, which leads to the premature closure of the coronal suture in the skull. This leads to an abnormally shaped skull and can cause various symptoms such as headaches, hearing difficulties, and developmental delays. There are no known synonyms for Muenke syndrome, as it is a specific condition with a specific genetic mutation causing it. Proper diagnosis and management can help affected individuals lead healthy and productive lives.
