Results 31 to 40 of about 1,191,732 (153)
Melkersson-rosenthal syndrome associated with hemifacial spasm [PDF]
, 2017 Melkersson-Rosenthal Syndrome, with findings of repeating facial paralysis, orofacial edema, and fissured tongue, is rarely seen clinically. We present the case of a 49-year-old female patient diagnosed with Melkersson-Rosenthal Syndrome, with the ...
Komurcu, Hatice Ferhan, Anlar, Omer
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Rossolimo–Melkersson–Rosenthal syndrome in a 12-year-old adolescent: report of a rare case
Клинический разбор в общей медицине, 2021 Rossolimo–Melkersson–Rosenthal syndrome is quite rare in children and adolescents 3–4 to 12–16 years of age. It most commonly occurs as a monosymptom in the form of macrocheilia.
Larisa I. Glebova +2 more
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A rare case of Melkersson–Rosenthal syndrome
Medical 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
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A Case of Melkersson-Rosenthal Syndrome Treated With 5-FU
Ear, Nose & Throat Journal, 2021 The rarity of Melkersson-Rosenthal syndrome, or orofacial granulomatosis, can present with persistent midface bogginess. The management for previous reported cases has included corticosteroid injections, antihistamines, and antibiotics.
David M. Alessi MD +2 more
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Melkersson‐Rosenthal‐syndrome ‐ A Rare Case of Laryngeal Involvement
, 2022 The Laryngoscope, Volume 132, Issue 12, Page 2442-2444, December 2022.
Nina Wenda +4 more
wiley +1 more source
Cheilitis granulomatosa (Miescher granulomatous macrocheilitis) with Down syndrome: A rare alliance
Indian 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
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Rossolimo–Melkersson–Rosenthal syndrome in 14 years old child with Down`s syndrome. Case report
, 2023 Rossolimo–Melkerson–Rosenthal syndrome is not so often diagnosed in childhood. It is noted that children's syndrome occurs as a monosymptom in the form of macrocheilitis.
Ekaterina V. Zadionchenko +1 more
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Syndrome de Melkersson-rosenthal: une entité rare à ne pas méconnaitre
The 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
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Allergy, Volume 81, Issue 8, Page 2744-2774, August 2026.ABSTRACT Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare disease characterized by unpredictable episodes of tissue swelling (angioedema), which, in most cases, occur first under the age of 18 years, and entail a significant burden of disease not only for the patients but also for their families.
Henriette Farkas +128 more
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Melkersson–Rosenthal Syndrome: A Case Report
Southern 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
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