EC Clinical and Medical Case Reports

Clinical Image Volume 8 Issue 9 - 2025

Post Natal Diagnosis of Crouzon Syndrome: About A Case

Benabdeslam Rim*, Anibri Mouna, Mchichou Sofia, Laaboudi Rim and El Hassouni Fatima

Department of Obstetrics and Gynecology, Oncology and High Risk Pregnancy, Souissi Maternity Hospital, Mohammed V University Rabat, Morocco

*Corresponding Author: Benabdeslam Rim, Department of Obstetrics and Gynecology, Oncology and High Risk Pregnancy, Souissi Maternity Hospital, Mohammed V University Rabat, Morocco.
Received: April 11, 2025; Published: August 07, 2025



Craniosynostosis is a premature closure of intracranial sutures with an incidence of 1/2000 births.

 Syndromic craniosynostosis corresponds to a single mutation with autosomal dominant transmission. However, the same gene can manifest with several phenotypes and conversely, the same phenotype can implicitly reveal several genes.

Benabdeslam Rim. “Post Natal Diagnosis of Crouzon Syndrome: About A Case”. EC Clinical and Medical Case Reports  8.9 (2025): 01-02.

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