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Journals / Ege Tıp Dergisi / 2017 / Cilt: 56 - Sayı: 1

Charcot-Marie-Tooth disease and bilateral abducens nerve palsy

Charcot-Marie-Tooth hastalığı ve bilateral abdusens sinir felci

Ebru Demet AYGIT
Osman Bulut OCAK
Aslı İNAL
Pages
44–46
DOI
—
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AI Summary & Key Takeaways

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

In this paper, it is aimed to report bilateral abducens nerve palsy involvement in CMT disease.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Charcot-Marie-Tooth (CMT) disease is the most common hereditary degenerative disorder of the peripheral nervous system.
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Key Findings & Data:It is generally inherited in an autosomal dominant pattern.
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Conclusion & Impact:In this paper, it is aimed to report bilateral abducens nerve palsy involvement in CMT disease.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Charcot-Marie-Tooth (CMT) disease is the most common hereditary degenerative disorder of the peripheral nervous system. It is generally inherited in an autosomal dominant pattern. Clinical diagnosis is based on family history and characteristic findings on physical examination. Cranial nerve involvement is rare. In this paper, it is aimed to report bilateral abducens nerve palsy involvement in CMT disease.

Özet

Charcot-Marie-Tooth (CMT) hastalığı, periferik nervöz sistemin en sık görülen dejeneratif bir hastalığıdır. Genellikle otozomal dominant olarak kalıtılır. Tanı, aile öyküsü ve fizik muayenedeki karakteristik bulgulara dayanır. Kraniyal sinir tutulumu nadir görülür. Bu yazıda, bilateral altıncı sinir tutulumu olan CMT hastalığının sunulması amaçlandı.

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Cite This Article

AYGIT, E. D., OCAK, O. B., İNAL, A. (2017). Charcot-Marie-Tooth disease and bilateral abducens nerve palsy. Ege Tıp Dergisi, Cilt: 56 - Sayı: 1, 44–46. https://ajindex.com/articles/190212

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References (1)

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