Медицинский вестник Юга России (Jun 2016)

A CASE OF THE HEREDITARY EPIDERMOLYSIS BULLOSA IN A NEWBORN CHILD

  • A. A. Afonin,
  • A. A. Lebedenko,
  • A. V. Shokarev,
  • T. B. Kozureva,
  • T. D. Tarakanova

DOI
https://doi.org/10.21886/2219-8075-2016-2-75-78
Journal volume & issue
Vol. 0, no. 2
pp. 75 – 78

Abstract

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We want to present a case of the hereditary epidermolysis bullosain a newborn child. The peculiarity of this case is the complicated clinical course of this syndrome in a newborn child generated by congenital herpes infectionsand hypoxic affections of the central nervous system. Today there are no ethiopathogenetic treatment methods for treating hereditary epidermolysis bullosa. All available treatment methods are symptomatic and are mainly aimed at patient care.

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