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Journals / Annals of Health Sciences Research / 2013 / Cilt: 2 - Sayı: 2

Papillon Lefevre Syndrome and Oral Findings in Pediatric Patient: A Rare Case Report

Pediatrik Bir Hastada Papillon Lefevre Sendromu ve Oral Bulguları: Nadir Bir Olgu Sunumu

Serkan DÜNDAR
Mustafa ERSÖZ
Eriş Sinan YÜCEL
Özge ÇELİK
Abubekir ELTAS
Pages
1–4
Publication Date
2013-10-01
DOI
—
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AI Summary & Key Takeaways

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

In this case, we aimed to present a rare PLS and its oral findings

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Papillon-Lefevre Syndrome PLS is a rare autosomal recessive disorder.
📊
Key Findings & Data:Cathepsin C Gene mutation are responsible for the etiology.
💡
Conclusion & Impact:In this case, we aimed to present a rare PLS and its oral findings
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Papillon-Lefevre sendromu · palmoplanter keratosis · periodontitis

Abstract

Papillon-Lefevre Syndrome PLS is a rare autosomal recessive disorder. Cathepsin C Gene mutation are responsible for the etiology. PLS characterized by palmoplantar keratosis and severe periodontal destruction in early ages, affecting the primary and permanent dentition. In this case, we aimed to present a rare PLS and its oral findings

Özet

Papillon-Lefevre Sendromu PLS nadir görülen otozomal resesif genetik geçişli bir hastalıktır. Etyolojisinde Cathepsin C Gen mutasyonu sorumlu tutulmaktadır. PLS, palmoplanter keratosis ve yaşamın erken dönemlerinde süt ve daimi dişleri etkileyen şiddetli doku yıkımıyla birlikte görülen periodontitis ile karakterizedir. Bu vakada PLS ve oral bulgularını sunmayı amaçladık

🔖

Cite This Article

DÜNDAR, S., ERSÖZ, M., YÜCEL, E. S., ÇELİK, Ö., ELTAS, A. (2013). Papillon Lefevre Syndrome and Oral Findings in Pediatric Patient: A Rare Case Report. Annals of Health Sciences Research, Cilt: 2 - Sayı: 2, 1–4. https://ajindex.com/articles/824894

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