Results 71 to 80 of about 1,191,732 (153)

Bilateral upper eyelid edema in Melkersson-Rosenthal syndrome

, 2005
8th Mediterranean-Ophthalmology-Society Congress -- 2004 -- Antalya, TURKEYMelkersson-Rosenthal syndrome is an uncommon disorder characterized by a triad of facial nerve palsy, orofacial edema, and fissured tongue.
Mukadder Koçak, Cengiz Akarsu, Sibel Erdoğan, Erdoğan, Sibel, Koçak, Mukadder, Pnar Atasoy, Akarsu, Cengiz, Atasoy, Pınar   +7 more
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Cheilitis granulomatosa: A case report with review of literature

Indian Journal of Dermatology, 2013
Cheilitis granulomatosa (CG) is a chronic swelling of the lip due to granulomatous inflammation. It is a rare inflammatory disorder first described by Miescher in 1945.
Nupura A Vibhute, Aniket H Vibhute, Nilima R Daule   +2 more
doaj   +1 more source

As a rare cause of recurrent facial nerve palsy: Mclkersson Rosenthal syndrome Yineleyen fasiyal sinir paralizisinin ender bir nedeni: Melkersson Rosenthal sendromu

, 2012
Melkersson-Rosenthal Syndrome is a granulomatous disease characterized by recurrent facial nerve paralysis, orofacial edema and fissured tongue. Observation of the classical triad is very rare and usually mono- oligosymptomatic involvement is observed. A
Saltik, Sema, Yüksel Karatoprak, Elif, Çetin, Ali Furkan   +2 more
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A Case of Melkersson, Rosenthal Syndrome

Eurasian Journal of Medicine, 2019
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Aves Editorial Aves Editorial
doaj  

Le syndrome de Melkersson-Rosenthal

, 2010
Le syndrome de Melkersson-Rosenthal est une affection rare, caractérisée dans sa forme complète par l'association d'un oedème facial, d'une paralysie faciale périphérique et d'une langue plicaturée.
KIMAKHE, Saïd, GOURE, Tony, CHEIKH, Samia   +2 more
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Melkersson Rosenthal Syndrome: a case report and review of the literature

, 2020
Melkersson Rosenthal Syndrome (MRS) is a rare neurological disorder characterized by swelling of the face, particularly one or both lips (granulomatous cheilitis), facial muscle weakness (palsy) and a fissured tongue. We present a patient with Melkersson
Edentalen, B.E., Osagie, R, Okoh, D, Okoh, M   +3 more
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Melkersson-Rosenthal Syndrome: A Case Study

, 2023
Melkersson-Rosenthal Syndrome (MRS) is a rare neuro-mucocutaneous disorder with unknown aetiology. It is classically characterised by a triad of signs: recurrent episodes of facial palsy, orofacial oedema and a fissured tongue, although it is uncommon ...
Michael Horley; Antigoni Koukkoulli
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Melkersson Rosenthal's syndrome in four generations

, 1979
Melkersson Rosenthal's syndrome is a rare condition, the hereditary nature of which is still in dispute. A family with seven affected members in four generations is described, which provides further evidence for the genetic basis of the ...
Tsakanikas, C., Vassilopoulos, D., Lygidakis, C., Illias, A.   +3 more
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Melkersson-Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants? [PDF]

Genes (Basel), 2023
Azzarà A, Cassano I, Lintas C, Pilato F, Capone F, Di Lazzaro V, Gurrieri F.   +6 more
europepmc   +1 more source

From Headache to Melkersson-Rosenthal Syndrome: A Case Report

International audienceMelkersson-Rosenthal syndrome is described as a syndrome which associates three cardinal signs: peripheral facial paralysis, facial oedema, and fissured tongue. These signs are rarely all present.
Schoenlaub, P., Legeas, C., Saucereau, Justine, Quere, Baptiste, Devauchelle-Pensec, Valérie   +4 more
core   +1 more source