✨
AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
We present a male infant who has HED with bilateral athelia, because it is rarely seen.
📌 3 Key Takeaways
🎯
Objective & Hypothesis:Hypohidrotic ectodermal dysplasia (HED) shows X-linked recessive inheritance in almost all cases.
📊
Key Findings & Data:The main features are hypotrichosis, absent or reduced sweating and partial or total anodontia.
💡
Conclusion & Impact:We present a male infant who has HED with bilateral athelia, because it is rarely seen.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Hypohidrotic ectodermal dysplasia (HED) shows X-linked recessive inheritance in almost all cases. The main features are hypotrichosis, absent or reduced sweating and partial or total anodontia. We present a male infant who has HED with bilateral athelia, because it is rarely seen.
Özet
Hipohidrotik ektodermal displazi, olguların hemen tümünde X'e bağlı geçiş göstermektedir. Başlıca özellikleri, hipotrikoz, azalmış veya tamamen kaybolmuş terleme ve parsiyel veya tam anodontiya'dır. Nadir görülmesi sebebiyle, bilateral meme başı yokluğu gösteren hipohidrotik ektudermal displazili bir erkek infant sunuyoruz.
🔖
Cite This Article
DOĞAN, B., HARMANYERİ, Y., TAŞKAPAN, O. (2022). Hypohidrotic ectodermal dysplasia with bilateral athelia: A case report. Türkderm-Deri Hastalıkları ve Frengi Arşivi, Cilt: 36 - Sayı: 3, 211–212. https://ajindex.com/articles/622281