cris.boxmetadata.label.title
Epidermolysis bullosa and congenital skin aplasia (Bart's syndrome). Report of 3 cases
cris.boxmetadata.label.alternativetitle
[Epidermolisis bulosa y aplasia cutis congénita (síndrome de Bart). Reporte de tres casos.]
cris.boxmetadata.label.dateissued
01 browse.startsWith.months.january 1988
cris.boxmetadata.label.accesslevel
metadata only access
cris.boxmetadata.label.resourcetype
journal article
cris.boxmetadata.label.authors
Peláez-Gutiérrez R.
Esparza-Urtecho W.
Meléndez-Guevara G.
Paoli-Razuri C.
Sánchez-Aznarán N.
cris.boxmetadata.label.abstract
The association of epidermolysis bullosa (EB), congenital localized absence of skin and nail alterations like anonychia and dystrophy has been denominated Bart's syndrome, which was described nineteen years ago, and associated with simple, junctional and dystrophies epidermolysis bullosa. We explain in this study three cases, which because of their clinic characteristics will correspond to this new entity. All of these cases happened in the city of Trujillo, Peru.
cris.boxmetadata.label.citationstartpage
149
cris.boxmetadata.label.citationendpage
154
cris.boxmetadata.label.volume
16
cris.boxmetadata.label.issue
2
cris.boxmetadata.label.language
Spanish
cris.boxmetadata.label.ocdeknowledgeArea
Dermatología, Enfermedades venéreas
cris.boxmetadata.label.scopusidentifier
2-s2.0-0023751092
cris.boxmetadata.label.pubmedidentifier
cris.boxmetadata.label.source
Medicina cutánea ibero-latino-americana
cris.boxmetadata.label.containerissn
02105187
peru-layout.shadow-copies
Directorio de Producción Científica
Scopus