Affiliation:
1. Kazan State Medical University;
City Clinical Hospital №7
2. Kazan State Medical University
Abstract
Congenital bullous epidermolysis is a severe hereditary disease, the main manifestation of which is bubbles that occur after minor mechanical action on the skin and mucous membranes due to congenital violation of the coding of dermo-epidermal proteins. The difficulty in making a diagnosis of congenital bullous epidermolysis is associated with the rarity of pathology and a small number of scientific publications.
Publisher
The National Academy of Pediatric Science and Innovation
Subject
Pediatrics, Perinatology and Child Health
Reference11 articles.
1. Congenital bullous epidermolysis. Guidelines No.100. Moscow Department of Health, 2018. (in Russ)
2. Drodina M.B., Koshkin S.V., Zukhur I.I., Bobro V.A. Clinic, diagnosis and treatment of epidermolysis bullosa. Immunopatologiya, allergologiya, infektologiya 2019; 4: 13–21. (in Russ.) DOI: 10.14427/jipai.2019.4
3. Dumchenko V.V., Tkachenko T.A., Bakhmutova E.G., Stepanova I.V., Lozovaya L.P., Vetoshkina L.N. A case of congenital dystrophic epidermolysis bullosa. Rossiiskii zhurnal kozhnykh i venericheskikh boleznei 2017; 20(1): 38–41. (in Russ.) DOI: http://dx.doi.org/10.18821/1560–9588–2017–20–1–38–41
4. Zverkova F.A. Skin diseases of young children. S-Pb.: Sotis, 1994; 120. (in Russ.)
5. Kotalevskaya Yu.Yu., Marycheva N.M. Bullous epidermolysis: the main clinical manifestations. Pediatriya 2014; 4: 70–72. (in Russ.)