Journals / Türkderm-Deri Hastalıkları ve Frengi Arşivi / 1999 / Cilt: 33 - Sayı: 4

Laugier-Hunziker syndrome

Laugier-Hunziker sindromu

Pages
255–257
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

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

The diseases in differential diagno-sis are evaluated by presenting two cases vvhich show the characteristics of this rare syndrome.

📌 3 Key Takeaways

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Objective & Hypothesis:Background and Design:Laugier- Hunziker t,ndrome is a benign, acçuired dermatosis characterized by 2- 5 mm wide, gray- brovvn- black macules on lips, Oral mucosa and nails.
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Key Findings & Data:Background and Design:Laugier- Hunziker t,ndrome is a benign, acçuired dermatosis characterized by 2- 5 mm wide, gray- brovvn- black macules on lips, Oral mucosa and nails.
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Conclusion & Impact:The diseases in differential diagno-sis are evaluated by presenting two cases vvhich show the characteristics of this rare syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background and Design:Laugier- Hunziker t,ndrome is a benign, acçuired dermatosis characterized by 2- 5 mm wide, gray- brovvn- black macules on lips, Oral mucosa and nails. The diseases in differential diagno-sis are evaluated by presenting two cases vvhich show the characteristics of this rare syndrome.

Özet

Laugıer- Hunziker sindromu dudaklar, oral mukoza ve tırnaklarda, 2- 5 mm çaplarda gri- kahverengi- siyah makulalar ile kendini gösteren, benign, edinsel bir dermatozdur. Oldukça nadir görülen bu sindroma ait özellikler gösteren iki olgu sunularak ayırıcı tanıya giren diğer sayrılıklar gözden geçirilmiştir.

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Cite This Article

GÜRLER, A. N., SOYAL, M. C., KUNDAK, S., AVCI, O. (2022). Laugier-Hunziker syndrome. Türkderm-Deri Hastalıkları ve Frengi Arşivi, Cilt: 33 - Sayı: 4, 255–257. https://ajindex.com/articles/622380

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