Journals / Endokrinolojide Yönelişler / 2000 / Cilt: 9 - Sayı: 3

Type I "Gaucher disease" showing intrafamilial characteristics

Ailevi özellik gösteren tip I "Gaucher hastalığı" olgusu

Pages
127–129
Publication Date
2022-10-17
DOI
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AI Summary & Key Takeaways

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

A 35 year old man showing typical presentation of the disease and with intrafamilial characteristics is discussed and the related literature has been reviewed.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:"Gaucher Disease" which is seen in more than one person in the same family is a rare case.
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Key Findings & Data:"Gaucher Disease" which is seen in more than one person in the same family is a rare case.
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Conclusion & Impact:A 35 year old man showing typical presentation of the disease and with intrafamilial characteristics is discussed and the related literature has been reviewed.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

"Gaucher Disease" which is seen in more than one person in the same family is a rare case. A 35 year old man showing typical presentation of the disease and with intrafamilial characteristics is discussed and the related literature has been reviewed.

Özet

Aynı ailenin birkaç bireyinde birden görülen "Gaucher Hastalığı" ender rastlanılan bir olgudur. Bu hastalığın karakteristik özelliklerini taşıyan 35 yaşında bir erkek hasta sunularak ilgili literatür gözden geçirildi.

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Cite This Article

ERTÜRK, N., SİPAHİOĞLU, F., TUNÇKALE, A., ERDAMAR, S., MADY, M., ÜNLÜSOY, Z., KARTEL, Y., YALDIRAN, A., ÖZTÜRK, E., AYATA, E. (2022). Type I "Gaucher disease" showing intrafamilial characteristics. Endokrinolojide Yönelişler, Cilt: 9 - Sayı: 3, 127–129. https://ajindex.com/articles/497601