Resumo

ELIZONDO, AD Pérez-  e  VALDES-LOPEZ, A. Bart syndrome: Report of a case. Rev. argent. dermatol. [online]. 2017, vol.98, n.4, pp.1-10. ISSN 1851-300X.

Bart syndrome is a rare congenital disorder characterized by the association of epidermolysis bullosa, localized congenital absence of skin and occasionally nail abnormalities. In this presentation we report the case of a male neonate referred to the Hospital para el Niño of IMIEM for evaluation of extensive blistering lesions and absence of skin in lower limbs, present from birth and who after treatment showed improvement, with a favorable clinical evolution.

Palavras-chave : Bart syndrome; aplasia cutis; epidermolysis bullosa.