In this article, the authors, referring to their own practice, cases from practice, present information about a rare syndrome in children - Melkersson-Rosenthal. Based on the results of their own clinical observation, instrumental and laboratory studies, the clinical and diagnostic criteria of the syndrome are described. Historical and modern literary data on the rare Melkersson-Rosenthal syndrome are provided. The authors argue that the disease begins during the transition from childhood to adolescence, and after treatment, the progression of the disease slows down, but does not stop, which requires close monitoring by both pediatricians and general practitioners.
| Mualliflar | Khamidov, Farrukhbek, Botirov, Kamolliddin, Khamidov, Asadbek, Хамидов, Фаррухбек, Ботиров, Камоллиддин, Хамидов, Асадбек, Xamidоv, Farruxbek, Botirov, Kamolliddin, Xamidоv, Asadbek |
|---|---|
| Jurnal | Халқаро илмий педиатрия журнали |
| Nashr sanasi | 2025-11-04 |
| Jild | 4 |
| Son | 5 |
| Betlar | 1133-1137 |
| Til | Rus |
| DOI | 10.56121/2181-2926-2025-4-5-1133-1137 |
DOI: 10.56121/2181-2926-2025-4-5-1133-1137 · Maqolaning asl sahifasi
синдром Мелькерссона-Розенталя, клиника, лечение, макрохейлит, гранулематозный хейлит, Melkersson-Rosenthal syndrome, clinical picture, treatment, macrocheilitis, granulomatous cheilitis, Melkersson-Rozental sindromi, klinik ko'rinishi, davolash, makroxeilit, granulomatoz cheilit
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