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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
The case is discussed under the light of the current literature.
📌 3 Key Takeaways
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Objective & Hypothesis:A 17 year-old female patient whose symptoms were in the form of progressive myoclonic epilepsia is presented.
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Key Findings & Data:A diagnosis of Unverricht Lundborg disease was made because of the typical clinical and electrophysiological findings.
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Conclusion & Impact:The case is discussed under the light of the current literature.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
A 17 year-old female patient whose symptoms were in the form of progressive myoclonic epilepsia is presented. A diagnosis of Unverricht Lundborg disease was made because of the typical clinical and electrophysiological findings. The case is discussed under the light of the current literature.
Özet
Progressif myoklonik epilepsi şeklinde seyreden ve Unverricht Lundborg hastalığı düşünülen 17 yaşında bayan hasta klinik ve elektrofizyolojik bulgularının tipik olması nedeniyle takdim edilmiş ve literatür bilgileri ışığında tartışılmıştır.
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Cite This Article
TALASLIOĞLU, A., ERSOY, A. Ö., KÖSEOĞLU, E., KAHRAMAN, Y. (2022). A case of Unverricht Lundborg disease. Erciyes Tıp Dergisi, Cilt: 24 - Sayı: 2, 86–90. https://ajindex.com/articles/502889