Crouzon's syndrome: A review of literature and case report

• Ngā kaituhi matua: Vivek Padmanabhan (Author), Amitha M Hegde (Author), Kavita Rai (Author)
• Hōputu: Pukapuka
• I whakaputaina: Wolters Kluwer Medknow Publications, 2011-01-01T00:00:00Z.
• Ngā marau: article
• Urunga tuihono: Connect to this object online.

Crouzon's syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder. Crouzon's syndrome is caused by mutation in the fibroblast growth factor receptor 2 (FGFR2) gene. Normally, th...