A CASE OF CONGENITAL EPIDERMOLYSIS BULLOSA IN A NEWBORN CHILD
DOI:
https://doi.org/10.34689/071j8804Keywords:
.Abstract
The article describes a case of congenital epidermolysis bullosa in a newborn child. This is a rare genetic skin disorder. The course and prognosis of the disease depend on its form. Children suffering from epidermolysis bullosa should be under regular medical supervision of a pediatrician, dermatologist, and orthopedic specialist.
References
К.К. Джаксалыкова, К.Д. Абаева, М.А. Имаханова СЛУЧАЙ ВРОЖДЕННОГО БУЛЛЕЗНОГО ЭПИДЕРМОЛИЗА У НОВОРОЖДЕННОГО РЕБЕНКА. //НАУКА ЗДРАВООХРАНЕНИЕ 2012.№ 4. С. 87-88 K. K. Zhaksalykova, K. D. Abayeva, M. A. Imahanova THE CASE OF CONGENITAL BULLOUS EPIDERMOLYSIS AT NEWBORN. // NAUKA I DRAVOOKHRANENIE 2012.№ 4. С. 87-88 К.Қ. Жақсылықова, К.Д. Абаева, М.А. Имаханова ЖАҢА ТУҒАН НӘРЕСТЕДЕГІ ТУМА БУЛЛЕЗДІ ЭПИДЕРМОЛИЗ ЖАҒДАЙЫ. // ҒЫЛЫМ ЖӘНЕ ЕНСАУЛЫҚ САҚТАУ. 2012.№ 4. С. 87-88
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Copyright (c) 2026 Куляш Джаксалыкова, Кадиша Абаева, М.А. Имаханова (Автор)
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