Results 61 to 70 of about 1,199,438 (182)

Morbihan disease: a case report and differentiation from Melkersson-Rosenthal syndrome [PDF]

, 2020
We present a 32-year old woman with a 9-year history of upper facial swelling. A workup by the ophthalmology department led to the diagnosis of Melkersson-Rosenthal syndrome.
Kuraitis, Drew, Wang, Alun, Coscarart, Aimee, Williams, Laura   +3 more
core   +1 more source

Nawracające porażenie nerwu twarzowego w przebiegu zespołu Melkerssona‑Rosenthala. Studium przypadku

Logopedia Silesiana, 2016
This case study describes an example of a rare disorder which applies to alternating facial nerve palsy in Melkersson-Rosenthal Syndrome. The first description of this case was published in 1928, when Ernst G.
Aleksandra Strach‑Sączewska
doaj  

Melkersson-Rosenthal syndrome: highlighting a diagnostic dilemma and future insights for a well-established genetic basis. A literature review

Journal of Rare Diseases
Purpose Melkersson-Rosenthal syndrome is a rare disorder characterized by a triad of recurring orofacial swelling, fissured tongue and recurring facial palsy.
Aliaa Abdelmoniem Bedeir Eita
doaj   +1 more source

Hypothyroidism presenting as a fissure tongue

Clinical Case Reports, Volume 12, Issue 3, March 2024.
Key Clinical Message We are reporting a case of hypothyroidism presenting as fissured tongue, demonstrating significant resolution of fissure tongue upon thyroid hormone replacement therapy.
Ravishankar Mylaraiah, Sangeeta Sharma, Tamer Shalaby   +2 more
wiley   +1 more source

Investigations into the aetiopathogenesis of orofacial granulomatosis using multiple omics technologies reveal a potential role for B cells

Clinical and Translational Medicine, Volume 16, Issue 5, May 2026.
Maria Tumelty, Krupali Patel, Helen Petersen, Chris Delaney, David Lappin, John Gibson, Gordon Ramage, Christopher van der Gast, Andrew Smith, Christopher John Nile   +9 more
wiley   +1 more source

A new gene for autosomal dominant facial palsy/migraine identified in a family by whole exome sequencing

European Journal of Neurology, Volume 31, Issue 1, January 2024.
Abstract Background Facial palsy manifests as unilateral or bilateral weakness and inability to move some of the facial muscles. The aetiology may be different including idiopathic, trauma, infections or brain tumours or it can be associated with chronic neurological diseases.
Alessia Azzarà, Ilaria Cassano, Carla Lintas, Laura Bernardini, Fabio Pilato, Fioravante Capone, Vincenzo Di Lazzaro, Fiorella Gurrieri   +7 more
wiley   +1 more source

Orofacial Granulomatosis among Pediatric Patients Well Controlled by Corticosteroid Treatment: A Rare Case Series

Case Reports in Pediatrics, Volume 2024, Issue 1, 2024.
Orofacial granulomatosis (OFG) is a rare disease entity characterized by nonnecrotizing granulomatous inflammation in the oral and maxillofacial regions, typically characterized by recurrent or persistent edema, primarily in the lips and occasionally in the gingiva. OFG is often associated with Crohn’s disease and sarcoidosis, and an accurate diagnosis
Taku Kimura, Ken-Ichiro Sakata, Shunichiro Takezaki, Takuya Asaka, Shohei Oshima, Aya Yanagawa-Matsuda, Yoshimasa Kitagawa, Paul A. Rufo   +7 more
wiley   +1 more source

Melkersson Rosenthal syndrome: a histopathologic mystery and dermatologic challenge

, 2015
Kaminagakura E, Jorge J Jr.
Jorge, J, Kaminagakura, E
core   +1 more source

Melkersson-Rosenthal sindrom [PDF]

Scripta Medica, 2014
Melkersson-Rosenthal syndrome (MRS) is manifested by recurrent edema in the region of the face or oral cavity, paralysis of facial muscles and fissured tongue. It is a rare, granulomatous disease of unknown cause.
Tadić Daliborka, Đajić Vlado, Miljković Siniša, Nazalević Majda, Popović Ljiljana   +4 more
doaj