Open AccessDystrophic type of autosomal dominant bullous epidermolysis in a newborn
Author(s) -
Н. И. Захарова,
В. А. Янин,
В. Л. Крикунова,
В. М. Хлебушкина,
О. С. Гаврилова
Publication year - 2019
Publication title -
rossijskij vestnik perinatologii i pediatrii
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.139
H-Index - 4
eISSN - 2500-2228
pISSN - 1027-4065
DOI - 10.21508/1027-4065-2019-64-3-78-81
Subject(s) - medicine , epidermolysis bullosa , dermatology , feature (linguistics) , pediatrics , philosophy , linguistics
The article presents the data of the clinical observation of a newborn with congenital bullous epidermolysis. The feature of this case is the course of this disease in the newborn with retardation of intrauterine development. Nowadays there is no aetiopathogenetic treatment of patients with inborn bullous epidermolysis and all existent methods of treatment of such patients are palliative. This study demonstrated a significant improvement of the baby’s clinical status.