2013, Number 5
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Med Cutan Iber Lat Am 2013; 41 (5)
Bart syndrome: congenital aplasia cutis and epidermolysis bullosa
Luján SM, García GRG, Álvarez CJP, Uribe PCJ
Language: Spanish
References: 14
Page: 218-222
PDF size: 667.73 Kb.
ABSTRACT
Aplasia cutis has been associated with the main subtypes of bullous epidermolysis, receiving the name of Bart syndrome. It mainly affects one lower
limb with a characteristic absence of skin with a S-shaped pattern plus bullous epidermolysis lesions elsewhere in the body. We present the case of a
pre-term male infant with all the clinical features mentioned investigated in the Neonatology Service of the Fundación Cardiovascular de Colombia,
Floridablanca, Colombia.
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