Servicios Personalizados
Revista
Articulo
Links relacionados
Compartir
Archivos de Medicina Interna
versión impresa ISSN 0250-3816versión On-line ISSN 1688-423X
Resumen
TABARES, Fernando; DIAZ, Carolina; MAS, Valentina y MONTEGHIRFO, Raquel. Congenital epidermolysis bullosa: report of a case. Arch. Med Int [online]. 2015, vol.37, n. 3, pp.135-139. ISSN 0250-3816.
Abstract: Epidermolysis bullosa is an hereditary, chronic,disease, incurable and with very low prevalence. It is characterized by blisters after minor trauma, with predominantly cutaneous manifestation and difficult manage. Interferes with the quality of life of patients requiring a multi-disciplinary therapeutic approach. We present a clinical case, in order to describe clinical manifestations, current diagnostic approach and therapeutic possibilities for the comprehensive management of patients with this disease.
Palabras clave : epidermolysis; bullous disease; congenital disease.