Resumo

VIDAL, Gimena; CARRAU, Fernanda; LIZARRAGA, Mariana  e  ALVAREZ, Mariela. Epydermolisis bullosa, one clinical case. Arch. Pediatr. Urug. [online]. 2018, vol.89, n.6, pp.382-388. ISSN 0004-0584.  https://doi.org/10.31134/ap.89.6.4.

Epidermolysis bullosa (EB) is a group of infrequent genodermatoses characterized by cutaneous fragility and blisters or erosions after minor skin trauma. This paper presents the case of a 15-day-old breastfed infant diagnosed with Epidermolysis Bullosa Simplex (EBS), it was based on clinical manifestations and electron microscopy evidence and had a subsequent favourable evolution. The case illustrates an infrequent disease and demonstrates the relevance of providing appropriate treatment immediately after childbirth, as well as the value of a multidisciplinary approach to the disease, since it has a high impact on the patients' quality of life.

Palavras-chave : Skin disease; Epidermolysis bullosa; Therapeutics; Genetic.

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