Crouzon Syndrome A Case Report

Crouzon syndrome is the most common syndrome in the craniosynostosis group. Crouzon syndrome accounts for about 4.8 of all cases. It usually has autosomal dominant inheritance with full penetrance and variable expressiveness from subtle to severe forms and is caused by maxillary hypoplasia with craniosynostosis, proptosis, and relative mandibular protrusion. be characterized. Mutations in the fibroblast growth factor receptor 2 gene have been implicated in the development of this rare genetic disorder. Our work reports the diagnosis of this rare syndrome in young patients based on clinical and radiological features. Prompt and timely treatment of the syndrome has allowed this patient to lead a normal life despite the syndrome. Dr. Kala Barathi. S | Mr. Azrudheen. B "Crouzon Syndrome: A Case Report" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-7 | Issue-1 , February 2023, URL: https://www.ijtsrd.com/papers/ijtsrd53851.pdf Paper URL: https://www.ijtsrd.com/medicine/nursing/53851/crouzon-syndrome-a-case-report/dr-kala-barathi-s