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Journals / Bağcılar Tıp Bülteni / 2019 / Cilt: 4 - Sayı: 2

Anesthesia Experience in a Patient with Myotonia Congenita

Konjenital Miyotonili Bir Hastadaki Anestezi Deneyimimiz

Yeşim Cokay ABUT
Serkan ŞİMŞEK
Seher KÖSE
Şenay KIRGEZEN
Kübra BOLAT
Veysel ERDEN
Pages
53–55
Publication Date
2022-10-12
DOI
—
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AI Summary & Key Takeaways

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

We presented our anesthesia experiencein a patient who suffers from MC in this article

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Myotonia congenita (MC) was first described as a skeletal muscledisorder by Thomsen in 1876.
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Key Findings & Data:As a result of the mutation of the chloridechannel gene (CLCN1), which is on the 17th chromosome, patients sufferfrom muscle contractility and fatigue.
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Conclusion & Impact:We presented our anesthesia experiencein a patient who suffers from MC in this article
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Myotonia congenita (MC) was first described as a skeletal muscledisorder by Thomsen in 1876. As a result of the mutation of the chloridechannel gene (CLCN1), which is on the 17th chromosome, patients sufferfrom muscle contractility and fatigue. Malignant hyperthermia may occurin these patients in anesthesia. We presented our anesthesia experiencein a patient who suffers from MC in this article

Özet

Myotoni konjenita (MC), Thomsen tarafından, 1876 yılında, iskelet kaslarında ortaya çıkan bir hastalık olarak tanımlanmıştır. On yedinci kromozomda yer alan klor kanalı geninin (CLCN1) bir mutasyonu sonucunda, hastalarda kas kontraksiyonları ve yorgunluk ortaya çıkar. Bu hastalarda anestezi altında malin hipertermi gelişebilir. Aşağıda bir MC hastasıyla ilgili olarak yaşadığımız anestezi deneyimini paylaşmak istiyoruz.

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Cite This Article

ABUT, Y. C., ŞİMŞEK, S., KÖSE, S., KIRGEZEN, Ş., BOLAT, K., ERDEN, V. (2022). Anesthesia Experience in a Patient with Myotonia Congenita. Bağcılar Tıp Bülteni, Cilt: 4 - Sayı: 2, 53–55. https://ajindex.com/articles/458995

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