Journals / Cukurova Medical Journal / 2014 / Cilt: 39 - Sayı: 4

A Case with Recurrent Facial Palsy: Melkersson-Rosenthal Syndrome

Tekrarlayan Fasiyal Paralizili bir olgu: Melkersson-Rosenthal Sendromu

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0
Publication Date
2014-07-22
DOI
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AI Summary & Key Takeaways

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

We present a 12 years-old male who is diagnosed Melkersson-Rosenthal syndrome.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Melkersson-Rosenthal syndrome (MRS) is a rare neuromucocutaneous syndrome characterized by recurrent facial paralysis, orofacial edema and fissured tongue.
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Key Findings & Data:Oligosymptomatic and monosymptomatic forms are more common than the triad.
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Conclusion & Impact:We present a 12 years-old male who is diagnosed Melkersson-Rosenthal syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Melkersson-Rosenthal sendromu · tekrarlayan fasiyal paralizi · çocuklar.

Abstract

Melkersson-Rosenthal syndrome (MRS) is a rare neuromucocutaneous syndrome characterized by recurrent facial paralysis, orofacial edema and fissured tongue. Oligosymptomatic and monosymptomatic forms are more common than the triad. The presence of two manifestations or one manifestation with granulomatous cheilitis in biopsy is sufficient to make diagnosis of Melkersson-Rosenthal syndrome. We present a 12 years-old male who is diagnosed Melkersson-Rosenthal syndrome.

Özet

Melkersson-Rosenthal sendromu (MRS), tekrarlayan fasiyal paralizi, orofasiyal ödem, dilde fissürle karakterize nadir bir nöromukokütanöz sendromdur. Oligosemptomatik ve monosemptomatik olgular, klasik triaddan sık görülür. Bulguların ikisinin görülmesi veya bulguların biri ve biyopside granülomatöz keilitin varlığı Melkersson-Rosenthal sendromu tanısı için yeterlidir. Bu yazıda Melkersson-Rosenthal sendromu tanısı alan 12 yaşında bir erkek sunulmuştur.

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Cite This Article

BULUT, D. F., MERT, G. G., İNCECİK, F., HERGÜNER, Ö. M., ALTUNBAŞAK, Ş. (2014). A Case with Recurrent Facial Palsy: Melkersson-Rosenthal Syndrome. Cukurova Medical Journal, Cilt: 39 - Sayı: 4, 0. https://ajindex.com/articles/56946

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