Abstract
Crouzon’s syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Crouzon’s syndrome is caused by mutation in the fibroblast growth factor receptor 2 (FGFR2) gene.. The disease is characterized by premature synostosis of coronal and sagittal sutures which begins in the first year of life. Case report of a male newborn is presented with characteristic features of Crouzon’s syndrome
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