Bart's syndrome is one among the lesser known presentations of epidermolysis bullosa. It is characterized by congenital localized bullae of skin and mucous membranes sometimes associated with nail deformities, all of which disappear during the neonatal period. Early recognition allows for avoidance of inappropriate systemic or local therapy.
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References
1.
Bart BJ, Gorlin RJ, Anderson VE, et al. Congenital localized absence of skin and associated abnormalities resembling epidermolysis bullosa. Arch Dermatol1966;93:296-304.
2.
Bauer EA, Briggaman RAThe mechanobullous diseases. In: Fitzpatrick TB, et al., eds. Dermatology in General Medicine . New York: McGraw-Hill, 1979, p. 336.
3.
Bart BJEpidermolysis bullosa and congenital localized absence of skin. Arch Dermatol1970; 101:78-81.
4.
Smith SZ, Cram DLA mechanobullous disease of the newborn. Arch Dermatol1978;114:81-4.
5.
Gedde-Dahl T. Jr. Sixteen types of epidermolysis bullosa . Acta Dermato-vener1981;Suppl. 95:74-87.