Results 61 to 70 of about 1,191,732 (153)

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 SYNDROME

Zdravniški Vestnik, 2004
Background. Granulomatous cheilitis is a rare chronic swelling of the lip due to granulomatous inflammation. Miescher cheilitis is the term used when the granulomatous changes are confined to the lip.
Valerija Balkovec, Maja Gabrič Zirkelbach   +1 more
doaj  

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  

Oligosymptomatic form of Melkersson-Rosenthal Syndrome possibly triggered by COVID-19 infection: A case report

Acta Marisiensis - Seria Medica
Melkersson Rosenthal syndrome (MRS) is a disease of multifactorial origin typically presented with a triad of symptoms including peripheral facial nerve paralysis, plicated tongue and orofacial edema.
Đuzelić Nisada, Čamdžić Nina, Durmišević Dževad, Rekić Amir, Hodžić Selma, Prohić Asja   +5 more
doaj   +1 more source

Melkersson–Rosenthal syndrome: A rare cause of recurrent facial palsy – A case report [PDF]

, 2020
Background: Melkersson–Rosenthal syndrome is a rare, neuro-mucocutaneous, granulomatous disorder of unknown etiology, clinically characterized by a triad of symptoms: recurrent facial nerve palsy, facial swelling and fissured tongue. Melkersson–Rosenthal
Zenebe Zewde, Yared
core  

Granulomatous Cheilitis of Miescher and Lingua Plicata as an Oligosymptomatic Form of Melkersson–Rosenthal Syndrome: Case Report and Review of Literature

Acta Medica Bulgarica
Granulomatous cheilitis of Miescher (GHM) is a rare chronic disorder that presents with recurrent swelling of one or both lips, frequently accompanied by erythema and edema of the whole face.
Bulanova S., Botev I., Krupev M., Dourmishev L.   +3 more
doaj   +1 more source

Miescher’s cheilitis: A case report with literature review

Journal of Pathology of Nepal, 2018
Miescher’s cheilitis is an inflammatory disorder characterized by chronic lip swelling due to granulomatous inflammation. It is rare disorder first described by Miescher in 1945. It is monosymptomatic form of Melkersson-Rosenthal syndrome.
Ram Chandra Adhikari, Mahesh Shah
doaj   +1 more source