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Journals / Anestezi Dergisi / 2003 / Cilt: 11 - Sayı: 4

Apert syndrome and anesthesia (Case report)

Apert sendromu ve anestezi (Olgu sunumu)

Karamehmet YILDIZ
Halit MADENOĞLU
Kudret DOĞRU
Adem BOYACI
Pages
302–304
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In our case presentation, we aimed to discuss the anesthetic method we applied to the patient with Apert syndrome, which was youngest case in the literature and to look over the literature knowledge related with this matter.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Apert Syndrome is a congenital illness characterised by craniosynostosis, maxillary hypoplasia and syndactyly.
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Key Findings & Data:Apert Syndrome is a congenital illness characterised by craniosynostosis, maxillary hypoplasia and syndactyly.
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Conclusion & Impact:In our case presentation, we aimed to discuss the anesthetic method we applied to the patient with Apert syndrome, which was youngest case in the literature and to look over the literature knowledge related with this matter.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Kraniyofasiyal anomaliler · Akrosefalosindaktili · Anestezi

Abstract

Apert Syndrome is a congenital illness characterised by craniosynostosis, maxillary hypoplasia and syndactyly. In our case presentation, we aimed to discuss the anesthetic method we applied to the patient with Apert syndrome, which was youngest case in the literature and to look over the literature knowledge related with this matter.

Özet

Apert Sendromu kranyosinostoz, maksillar hipoplazi ve sindaktili ile karakterize kongenital bir hastalıktır. Bu olgu sunumunda, aynı zamanda literatürde yer alan olguların en küçüğü olan (50 günlük), Apert sendromlu olgumuza uyguladığımız genel anestezi yönteminin tartışılması ve konu ile ilgili literatür bilgilerinin gözden geçirilmesi amaçlanmıştır.

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Cite This Article

YILDIZ, K., MADENOĞLU, H., DOĞRU, K., BOYACI, A. (2003). Apert syndrome and anesthesia (Case report). Anestezi Dergisi, Cilt: 11 - Sayı: 4, 302–304. https://ajindex.com/articles/355493

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References (10)

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