Results 11 to 20 of about 1,199,438 (182)
Melkersson-Rosenthal syndrome: a classical case report [PDF]
RGO: Revista Gaúcha de Odontologia, 2023 The Melkersson-Rosenthal syndrome constitutes a rare manifestation characterized by a triad of signs and symptoms: recurrent orofacial edema, fissured tongue, and recurrent facial paralysis.
Carina DOMANESCHI +4 more
doaj +3 more sources
Crohn’s Disease and the Melkersson-Rosenthal Syndrome [PDF]
Canadian 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 +2 more sources
Melkersson-Rosenthal Syndrome: A forgotten diagnosis
Vision Pan-America, 2012 The rare, non-caseating, granulomatous disease known as Melkersson-Rosenthal syndrome (MRS) can be diagnostically difficult especially when not presenting as the characteristic triad of facial palsy, facial edema, and fissured tongue.1 We present a case ...
Michael D. Karon +1 more
doaj +2 more sources
Melkersson–Rosenthal syndrome [PDF]
QJM: An International Journal of Medicine, 2017 Melkersson-Rosenthal sendromu, ağırlıklı olarak dudakları tutan tekrarlayan orofasyal ödem, tekrarlayan fasyal sinir paralizisi ve fissürlü dil triadı ile karakterize bir hastalıktır. Sıklıkla 2. dekatta ortaya çıkmaktadır. En sık görülen bulgu orofasyal
Placke, J. M. +2 more
core +8 more sources
A Case with Recurrent Facial Palsy: Melkersson-Rosenthal Syndrome
Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2014 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.
Derya Fatma Bulut +4 more
doaj +2 more sources
Melkersson-rosenthal syndrome: a case report. [PDF]
J Istanb Univ Fac Dent, 2017 Melkersson-Rosenthal Syndrome (MRS) is a rare disorder consisting of a triad of persistent or recurrent orofacial edema, relapsing facial paralysis and fissured tongue. It is rarely possible to observe all aspects of the classical triad at the same time, since these symptoms may appear in different times of life cycle.
Basman A +4 more
europepmc +7 more sources
Syndrome de Melkersson-Rosenthal [PDF]
The 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 +2 more sources
Melkersson–Rosenthal syndrome: a case report of a rare disease with overlapping features [PDF]
Allergy, Asthma & Clinical Immunology, 2019 Background Melkersson–Rosenthal syndrome (MRS) is a rare, neuro-mucocutaneous disease which presents as orofacial swelling, facial palsy and fissured tongue.
Mauro Cancian +6 more
doaj +2 more sources
Management Strategies of Melkersson-Rosenthal Syndrome: A Review [PDF]
International Journal of General Medicine, 2020 Sumeet R Dhawan,1 Arushi G Saini,2 Pratibha D Singhi2,3 1Department of Pediatrics, Maharishi Markandeshwar Institute of Medical Sciences and Research, Mullana, Ambala, 133207, India; 2Pediatric Neurology Unit, Department of Pediatrics, Postgraduate ...
Dhawan SR, Saini AG, Singhi PD
doaj +2 more sources
Melkersson-Rosenthal syndrome associated to Hashimoto’s thyroiditis
Iberoamerican Journal of Medicine, 2020 Melkersson-Rosenthal syndrome (MRS) is a rare neuromucocutaneous granulomatous disorder classically defined by the triad: fissured tongue (lingua plicata), recurrent orofacial edema, and relapsing facial paralysis.
Salem Bouomrani +2 more
doaj +4 more sources