Journals / Nöropsikiyatri Arşivi / 2014 / Cilt: 51 - Sayı: 1

Akut motor iletim bloğu nöropatisi: Guillain-barre sendromu varyantı

Acute motor conduction block neuropathy: Another distinct variant of guillain-barre syndrome

Pages
82–85
DOI
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AI Summary & Key Takeaways

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

At the 28th week, the clinical examinationand electrophysiological findingsshowed complete recovery.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:We describe a patient who developed progressive weakness in all limbs without sensory symptoms 4 weeks after upper respiratory system infection.
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Key Findings & Data:Electrophysiological studies were performed at admission, 12th and 28th weeks.
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Conclusion & Impact:At the 28th week, the clinical examinationand electrophysiological findingsshowed complete recovery.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

We describe a patient who developed progressive weakness in all limbs without sensory symptoms 4 weeks after upper respiratory system infection. Electrophysiological findings suggested a new variant of Guillain-Barré syndrome named “acute motor conduction block neuropathy”. Electrophysiological studies were performed at admission, 12th and 28th weeks. At the 28th week, the clinical examinationand electrophysiological findingsshowed complete recovery.

Özet

Olgumuz üst solunum sistemi enfeksiyonundan 4 hafta sonra gelişen, duyu bozukluğu olmaksızın progresif seyirli dört ekstremite güçsüzlüğü ile prezente olmuştur. Elektrofizyolojik bulgular nadir bir Guillain-Barre sendromu varyantı olan“akut motor iletim bloğu nöropatisi” ile uyumlu bulunmuştur. Elektrofizyolojik çalışmalar 12. ve 28. haftada tekrar edildi. 28. haftada hastanın klinik ve elektrofizyolojik bulguları tamamen düzelmiş olarak bulundu.

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Cite This Article

ERDOĞMUŞ, N. İ., ÖZTEKİN, M. F., ÖZTEKİN, N. (2014). Akut motor iletim bloğu nöropatisi: Guillain-barre sendromu varyantı. Nöropsikiyatri Arşivi, Cilt: 51 - Sayı: 1, 82–85. https://ajindex.com/articles/292463

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