✨
AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
In this article, we present a new case reviewing all cases in Turkish literature.
📌 3 Key Takeaways
🎯
Objective & Hypothesis:Dyskeratosis congenita is a rare inherited disorder with abnormalities in the skin, mucous membranes, and bone marrow.
📊
Key Findings & Data:Most cases are X-linked, but autosomal dominant and recessive forms of the disease also declare.
💡
Conclusion & Impact:In this article, we present a new case reviewing all cases in Turkish literature.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Dyskeratosis congenita is a rare inherited disorder with abnormalities in the skin, mucous membranes, and bone marrow. Most cases are X-linked, but autosomal dominant and recessive forms of the disease also declare. In this article, we present a new case reviewing all cases in Turkish literature.
Özet
Diskeratozis konjenita, deri, muköz membran ve kemik iliği tutulumu gösterebilen ender görülen genetik geçişli bir hastalıktır. Çoğu olgu X' e bağlı geçiş özelliği gösterse de otozomal ve resesif formlar da bildirilmiştir. Bu makalede, yeni bir olgu sunulmuş ve Türk dermatoloji literatüründeki tüm olgular da gözden geçirilmiştir.
🔖
Cite This Article
KÖSE, O., TAŞTAN, B., GÜR, A. R., KURUMLU, Z. (2022). Dyskeratosis congenita (A retrospective study in Turkish dermatologic literature). Türkderm-Deri Hastalıkları ve Frengi Arşivi, Cilt: 34 - Sayı: 4, 239–241. https://ajindex.com/articles/622343