2017, Number 2
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Rev Med MD 2017; 8.9 (2)
Bart's Syndrome
Pérez-Elizondo AD, Valdés-López A
Language: Spanish
References: 7
Page: 187-190
PDF size: 529.53 Kb.
ABSTRACT
Bart's syndrome is an infrequent congenital disorder characterized by the association of epidermolysis bullosa,
localized congenital skin absence, and occasional nail abnormalities. In this report, we describe the case of a male
newborn that was sent to the Children's Hospital at the Maternal and Child Institute of the State of Mexico to receive
assessment. At his arrival medical examination revealed extended blisters and localized congenital skin absence in
lower limbs at birth. After treatment the patient experienced notorious improvement and a favorable clinical evolution.
REFERENCES
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Denizmen A, Yilmaz E, Citak A, Kurt A, Elkiran O, Okur I, Ozercan I. Aplasia cutis congenita and epidemolysis bullosa: Bart sindrome. Int J Dermatol 2010; 49: 343-5
McCarthy MA, Clarke T, Powell FC. Epidermolysis bullosa and aplasia cutis. Int J Dermatol 1991; 30: 481-4.
Prada J, Rojas L. Sindrome de Bart, Reporte de un caso. Revista Med 2008; 16: 232-6.
5.Sianez-Gonzalez C, Pezoa-Jares R, Salas-Alanis JC. Congenital epidermolysis bullosa: a review. Actas Dermosifiliogr 2009; 100: 842-56.
Frieden IJ: Aplasia cutis congenital: a clinical review and proposal for classifi cation. J Am Acad Dermatol 1986; 14: 646-60.
Boente MC, Asial RA, Del Valle Frontini M, Primc NB, Winik BC. Epidermolisis Ampollar con Ausencia Congénita Localizada de piel (Síndrome de Bart). ¿Es posible hablar de pérdida de heterozigocidad? Dermatol Pediatr Lat 2004; 2(2): 125-129.