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Journals / Medical Network Klinik Bilimler ve Doktor / 2000 / Cilt: 6 - Sayı: 2

Pendred syndrome

Pendred sendromu

NAZİF ZEYBEK
Muammer GÖZAYDIN
Cem BÜYÜKÇAKIR
Pages
179–181
DOI
—
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AI Summary & Key Takeaways

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

Also, recent developments on the subject were reviewed.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:We present a case who has autosomal recessive inheritance deafness, dumbness and hypothyroid goiter.
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Key Findings & Data:This symptom group resembles Pendred syndrome which is rarely seen.
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Conclusion & Impact:Also, recent developments on the subject were reviewed.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Sağırlık · Guatr · Hipertiroidi

Abstract

We present a case who has autosomal recessive inheritance deafness, dumbness and hypothyroid goiter. This symptom group resembles Pendred syndrome which is rarely seen. Also, recent developments on the subject were reviewed.

Özet

Otozomal resesif geçişli sağırlığı, dilsizliği ve hipotiroid guatrı olan bir olgumuzu sunuyoruz. Pendred sendromu olarak bilinen bu olgulara literatürde az sayıda rastlandığından konu ile ilgili gelişmeler gözden geçirilmiştir.

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Cite This Article

ZEYBEK, N., GÖZAYDIN, M., BÜYÜKÇAKIR, C. (2000). Pendred syndrome. Medical Network Klinik Bilimler ve Doktor, Cilt: 6 - Sayı: 2, 179–181. https://ajindex.com/articles/279637

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