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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
We present a case of polymyositis with coexistence EB in this article.
📌 3 Key Takeaways
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Objective & Hypothesis:Polymyositis, characterized with proximal muscle weakness, elevated serum muscle enzymes, myopathic findings on electromyography and muscle biopsy, is an inlammatory myopathy.
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Key Findings & Data:Epidermolysis bullosa (EB) is a rare disease which is characterized with bullae formation.
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Conclusion & Impact:We present a case of polymyositis with coexistence EB in this article.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Epidermolisiz bulloza simpleks · Polimiyozit · Epidermolysis Bullosa Simplex
Abstract
Polymyositis, characterized with proximal muscle weakness, elevated serum muscle enzymes, myopathic findings on electromyography and muscle biopsy, is an inlammatory myopathy. Epidermolysis bullosa (EB) is a rare disease which is characterized with bullae formation. We present a case of polymyositis with coexistence EB in this article.
Özet
Polimiyozit, proksimal kas güçsüzlüğü, kas enzimlerinde yükseklik, elektromiyografide ve kas biyopsisinde miyopatik değişiklikler ile karakterize, inflamatuvar bir miyopatidir. Epidermolizis bulloza (EB) ise, bül oluşumuyla karakterize nadir bir hastalıktır. Burada, polimiyozit ile EB'nın birlikte görüldüğü bir olgu sunulmuştur.
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Cite This Article
AKSU, K., KISAKOL, G., İNAL, V., ATEŞ, U., OKSEL, F., KESER, G., ÖZTÜRK, G., TÜZÜN, M., DOĞANAVŞARGİL, E. (2002). Polimiyozit ve epidermolizis bulloza simplex birlikteliği (Weber-cockayne varyantı): Olgu sunumu. Ege Tıp Dergisi, Cilt: 41 - Sayı: 1, 43–45. https://ajindex.com/articles/223378