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Crouzon Syndrome: a fibroblast growth factor receptor 2 gene mutation

عنوان مقاله: Crouzon Syndrome: a fibroblast growth factor receptor 2 gene mutation
شناسه ملی مقاله: JR_SBMU-2-1_004
منتشر شده در شماره 1 دوره 2 فصل January در سال 1396
مشخصات نویسندگان مقاله:

Farhad Safari - Anesthesiology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Kamran Mottaghi - Anesthesiology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Rofeideh Fallahinejadghajari - Anesthesiology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Masoud Nashibi - Anesthesiology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran

خلاصه مقاله:
Crouzon syndrome is a rare autosomal dominant premature cranyosynostosis, caused by fibroblast growth factor receptor 2 gene mutation on chromosome 10. The predominant skull and facial malformations with potential compromised airway make the crouzon syndrome a demanding issue for anesthesiologists and surgeons, required dynamic team work. In this report we describe a child, a known case of Crouzon syndrome who was a candidate for optic nerve decompression through endoscopic surgery. The anesthetic considerations and management are presented.

کلمات کلیدی:
Crouzon Syndrome, FGFR2 gene, Difficult Intubation, Anesthesia

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/994805/