Literature DB >> 8302226

[Melkersson-Rosenthal syndrome. A case report].

M Pellegrino1, M R D'Altilia, M Pastore, F Frascolla, D Meleleo, L Zelante, F Lotti.   

Abstract

The Melkersson-Rosenthal syndrome is a rare disease of unknown pathogenesis. Classical signs include recurrent facial palsy, lingua plicata and orofacial edema. The diagnosis is often difficult when all features are not present at the same time: in the literature complete triads occurred in 25-30% of the patients. We report a case of Melkersson-Rosenthal syndrome with classical triad of signs in a 13 year old boy. The pathology, clinical features and management of this disease are discussed: the possible role of food allergy or additives intolerance is also examined.

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Year:  1993        PMID: 8302226

Source DB:  PubMed          Journal:  Minerva Pediatr        ISSN: 0026-4946            Impact factor:   1.312


  1 in total

1.  Melkersson-Rosenthal syndrome: a rare variant of the monosymptomatic form.

Authors:  Carolina Tagliari Estacia; Aluisio Rosa Gameiro Filho; Izadora Bouzeid Estacia da Silveira; Rodrigo Rosa Gameiro; Anna Laura Salabert Della Barba
Journal:  GMS Ophthalmol Cases       Date:  2022-02-08
  1 in total

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