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dc.contributor.author Dudnyk, V. M. en
dc.contributor.author Izumets, O. I. en
dc.contributor.author Rubina, O. S. en
dc.contributor.author Furman, V. H. en
dc.date.accessioned 2023-03-06T10:44:30Z
dc.date.available 2023-03-06T10:44:30Z
dc.date.issued 2021
dc.identifier.citation Inherted epidermolysis bullsa in newborn (case study) / V. M. Dudnyk, O. I. Izumets, O. S. Rubina, V. H. Furman // Wiadomosci Lecarskie. – 2021. – Vol. 74, issue 10(1). – P. 2025–2029. en
dc.identifier.uri https://dspace.vnmu.edu.ua/123456789/6070
dc.description.abstract Inherited epidermolysis bullosa(IEB) is a group of genetically and clinically heterogeneous diseases characterized by the formation on the skin and mucous membranes blisters and erosion due to injury. Different forms of IEB can be accompanied by various extracutaneous complications, such as blisters and erosion on the cornea and mucous membranes, stenoses and strictures of the respiratory system, gastrointestinal tract, urinary system, muscle dystrophy, and malignant tumors. Therefore diagnosis and prescribing appropriate treatment and follow-up care is an important task for eonatologists and pediatric dermatologists. Because the manifestations of IEB are numerous, a specialized center is required for optimal care, where multidisciplinary care will be provided (neonatologists, pediatric surgeons, pediatric dermatologists, etc.). The purpose of this case report is to pay attention of specialists to a disease that is rare, to present clinical case of IEB in newborn who was admitted to the intensive care unit of newborns of Vinnitsa Regional Children’s Clinical Hospital. en
dc.language.iso en en
dc.subject inherited epidermolysis bullosa en
dc.subject newborns en
dc.title Inherted epidermolysis bullsa in newborn (case study) en
dc.type Article en


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