EC Paediatrics

Review Article Volume 14 Issue 2 - 2025

Craniofrontonasal Syndrome: A Rare Genetic Pathology - A Case Study: Detailed Clinical and Genetic Study and Literature Review

B Elalaoui1*, S Aithmadouch2 and R Abilkacem2

1Children’s Hospital, Ibn Sina University Hospital Centre, Mohammed 5 University, Rabat, Morocco
2Hôpital Militaire d’Instruction Mohamed V, Morocco

*Corresponding Author: B Elalaoui, Children’s Hospital, Ibn Sina University Hospital Centre, Mohammed 5 University, Rabat, Morocco.
Received: January 03, 2025; Published: January 23, 2025



Isolated craniofacial dysplasia in children is a complex congenital anomaly characterized by malformations of the skull and face. This pathology can be influenced by specific genetic mutations. Here is an overview of the main aspects, focusing on the responsible genetic mutations, diagnosis, and therapeutic management.

 Keywords: Craniofrontonasal Syndrome; Genetic Pathology; Skull and Face

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B Elalaoui., et al. "Craniofrontonasal Syndrome: A Rare Genetic Pathology - A Case Study: Detailed Clinical and Genetic Study and Literature Review". EC Paediatrics 14.2 (2025): 01-07.