Craniosynostosis Muenke type

Muenke syndrome, also known as FGFR3-related craniosynostosis, is a human specific condition characterized by the premature closure of certain bones of the skull during development, which affects the shape of the head and face. First described by Maximilian Muenke, the syndrome occurs in about 1 in 30,000 newborns. [Source: Wikipedia ]

Synonyms
Muenke syndrome
OrphaNet reference
Muenke syndrome 
May Cause
Craniosynostosis