Melkersson-Rosenthal syndrome

Common Name(s)

Melkersson-Rosenthal syndrome

Melkersson-Rosenthal syndrome is a rare neurological disorder characterized by recurring facial paralysis, swelling of the face and lips, and the development of folds and furrows in the tongue. Onset is in childhood or early adolescence. After recurrent attacks, swelling may persist and increase, eventually becoming permanent. The lip may become hard, cracked, and fissured with a reddish-brown discoloration. The cause of Melkersson-Rosenthal syndrome is unknown, but there may be a genetic predisposition. It can be symptomatic of Crohn's disease or sarcoidosis.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Melkersson-Rosenthal syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Melkersson-Rosenthal syndrome" returned 18 free, full-text research articles on human participants. First 3 results:

[Melkersson-Rosenthal syndrome: a rare entity not to ignore].
 

Author(s): Rim Klii, Wafa Chebbi

Journal:

 

Last Updated: 25 Sep 2015

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[Melkersson-Rosenthal syndrome].
 

Author(s): Madiha Mahfoudhi, Khaled Khamassi

Journal:

 

Last Updated: 9 Mar 2016

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Tufted hair folliculitis associated with Melkersson-Rosenthal syndrome and hidradenitis suppurativa.
 

Author(s): Sule Güngör, Tülin Yüksel, Ilteris Topal

Journal: Indian J Dermatol Venereol Leprol. ;80(5):484.

 

Last Updated: 9 Sep 2014

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Melkersson-Rosenthal syndrome" returned 2 free, full-text review articles on human participants. First 3 results:

Melkersson-Rosenthal syndrome as an early manifestation of mixed connective tissue disease.
 

Author(s): Dorota Jasinska, Jerzy Boczon

Journal:

 

We aim to illustrate the potential viability of MCTD as an underlying aetiology of Melkersson-Rosenthal syndrome. The case is probably the first description available in the literature of the Melkersson-Rosenthal as an early manifestation of mixed connective tissue disease.

Last Updated: 24 Dec 2015

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[Macrocheilitis and Melkersson-Rosenthal syndrome. Review of 19 cases].
 

Author(s): C Marques, A Machado, A P Baptista

Journal: Acta Med Port. 1994 Oct;7(10):533-40.

 

Melkersson-Rosenthal syndrome is an uncommon condition of unknown cause. The classical triad includes recurrent orofacial oedema involving predominantly the lips (macrocheilitis), intermittent peripheral facial palsy and scrotal tongue. Some authors consider Miescher's cheilitis as ...

Last Updated: 16 Mar 1995

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.