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Journals / Journal of Clinical and Analytical Medicine / 2014 / Cilt: 5 - Sayı: 4

Walker Warburg Sendromlu Üç Olgu

Three Cases of Walker Warburg Syndrome

Adnan AYVAZ
Mehmet ATALAR
Ozan KOÇAK
Füsun Dilara İÇAĞASIOĞLU
Pages
338–340
Publication Date
2022-10-18
DOI
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AI Summary & Key Takeaways

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

According to our knowledge, one of our patients is the longest- lived case who has been reported.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Walker-Warburg syndrome (WWS), a rare form of congenital muscular dystrophy,is an autosomal recessive disorder affecting the brain, eye, and muscles.
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Key Findings & Data:In thisstudy, three WWS cases followed in the pediatric clinic of Cumhuriyet Universityare presented.
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Conclusion & Impact:According to our knowledge, one of our patients is the longest- lived case who has been reported.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Walker-Warburg syndrome (WWS), a rare form of congenital muscular dystrophy,is an autosomal recessive disorder affecting the brain, eye, and muscles. In thisstudy, three WWS cases followed in the pediatric clinic of Cumhuriyet Universityare presented. According to our knowledge, one of our patients is the longest- lived case who has been reported.

Özet

Walker Warburg Sendromu (WWS) otozomal resesif geçiş gösteren göz, beyin vekasların etkilendiği nadir bir doğumsal musküler distrofi tipidir. Bu yazıda Cumhuriyet Üniversitesi Çocuk Sağlığı ve Hastalıkları kliniğinde takip edilen üç WWS olgusu sunulmuştur. Olgularımızdan biri bilgilerimize göre rapor edilmiş en uzun yaşayan olgudur.

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Cite This Article

AYVAZ, A., ATALAR, M., KOÇAK, O., İÇAĞASIOĞLU, F. D. (2022). Walker Warburg Sendromlu Üç Olgu. Journal of Clinical and Analytical Medicine, Cilt: 5 - Sayı: 4, 338–340. https://ajindex.com/articles/561156

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References (7)

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