Results 11 to 20 of about 87 (51)

A rare case of Melkersson–Rosenthal syndrome

open access: yesMedical Journal of Dr. D.Y. Patil Vidyapeeth, 2021
Melkersson–Rosenthal syndrome (MRS) is a rare clinical syndrome. The onset of illness usually occurs in the second decade of life. It is characterized by idiopathic facial paralysis and/or fissured tongue with oro-facial swelling, mainly lip edema.
Rajesh Verma, Rohit Anand
doaj   +1 more source

Crohn’s Disease and the Melkersson-Rosenthal Syndrome

open access: yesCanadian Journal of Gastroenterology, 1999
A 30-year-old woman with a 10-year history of recurrent bloody diarrhea and documented colitis of the descending colon, consistent with Crohn’s disease, presented with an exacerbation of her gastrointestinal disease and an 18-month history of recurrent ...
Alexandra Ilnyckyj   +3 more
doaj   +1 more source

Cheilitis granulomatosa (Miescher granulomatous macrocheilitis) with Down syndrome: A rare alliance

open access: yesIndian Journal of Paediatric Dermatology, 2016
Melkersson–Rosenthal syndrome comprises of the triad of orofacial swelling, facial paralysis, and fissured tongue. It may present in monosymptomatic form as Meischer granulomatous cheilitis. Herein we report an unusual association of Meischer's cheilitis
Balwinder Kaur Brar   +2 more
doaj   +1 more source

Syndrome de Melkersson-rosenthal: une entité rare à ne pas méconnaitre

open access: yesThe Pan African Medical Journal, 2015
Le syndrome de Melkersson-Rosenthal est une entité clinique rare, définie par la triade oedème oro-facial, paralysie faciale récurrente et langue plicaturée. Cette triade peut être incomplète ou apparaître de manière différée dans le temps. Le diagnostic
Rim Klii, Wafa Chebb
doaj   +1 more source

Melkersson–Rosenthal Syndrome: A Case Report

open access: yesSouthern Clinics of Istanbul Eurasia, 2018
Melkersson-Rosenthal Syndrome (MRS) is a rare disease characterized by the triad of recurring facial paralysis, a fissured tongue, and recurring swelling of the lips and/or face.
Sedat Aydın   +4 more
doaj   +1 more source

Syndrome de Melkersson-Rosenthal

open access: yesThe Pan African Medical Journal, 2015
Le syndrome de Melkersson-Rosenthal est une entité rare. Dans sa forme complète, il se caractérise par un èdème cutanéo-muqueux de la face, une paralysie faciale périphérique récidivante et une langue plicaturée.
Madiha Mahfoudhi, Khaled Khamassi
doaj   +1 more source

Melkersson-Rosenthal Syndrome: a Case Report of the Classic Triad

open access: yesJournal of Dentistry, 2020
Melkersson-Rosenthal syndrome (MRS) is a rare neurological condition that includes a triad of symptoms including recurring facial paralysis, orofacial swelling, and fissured tongue.
Molook Torabi   +2 more
doaj   +1 more source

Presentation of Bilateral Facial Paralysis in Melkersson–Rosenthal Syndrome

open access: yesCase Reports in Neurological Medicine, 2021
Introduction. Melkersson–Rosenthal syndrome (MRS) is a neuromucocutaneous disorder characterized by the following classic symptom triad: peripheral facial paralysis, orofacial edema, and scrotal or fissured tongue.
Gustavo Gaitan-Quintero   +3 more
doaj   +1 more source

Complete clinical spectrum of melkersson–Rosenthal syndrome with bilateral temporal optic disc pallor – A case report

open access: yesTNOA Journal of Ophthalmic Science and Research, 2023
Melkersson Rosenthal syndrome (MRS) is a very rare neuro-mucocutaneous disease, the aetiology of which is not well defined. It is classically characterised by recurring facial paralysis, swelling of face, lips and presence of a furrowed tongue.
Henal Javeri   +5 more
doaj   +1 more source

Recurrent Facial Nerve Paralysis: A Case report on Melkersson-Rosenthal Syndrome

open access: yesJournal of Interdisciplinary Medicine, 2022
This is a case report of a 27-year-old male who presented with recurrent facial swelling and weakness. The clinical evaluation revealed that the patient had Melkersson-Rosenthal syndrome (MRS), a rare neurological disease characterized by the triad of ...
Sahadevan Mahavishnu   +3 more
doaj   +1 more source

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