Crouzon syndrome is a genetic disorder, autosomal dominant, characterized by the premature fusion of certain skull bones, which affects the shape of the head and face. It is caused by mutations in the FGFR2 gene, which in turn provides instructions for producing fibroblast growth factor receptor 2. The article presents a case of Crouzon’s syndrome in a female patient aged 40.

Key words: Crouzon syndrome, facial skull disorders, clinical syndromes.