A Case of Bart's Syndrome
Annals of Dermatology
; : 23-26, 2003.
Article
em En
| WPRIM
| ID: wpr-194040
Biblioteca responsável:
WPRO
ABSTRACT
Bart's syndrome was initially described as a genodermatosis characterized by congenital localized absence of the skin with blistering and nail deformities 1-3. However, it is considered as any type of epidermolysis bullosa(EB) with localized congenital absence of the skin on the extremities. A 33-day-old fbmale baby was presented with congenital absence of the skin over the left shin and dorsa of both feet which were covered with the thin, translucent, and brown-red glistening membranes. Blistering of the right calf and left great toe nail deformity were also noted. She was diagnosed as a recessive dystrophic EB by the histopathological, ultra- structural and immunomapping studies.
Palavras-chave
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Pele
/
Anormalidades Congênitas
/
Dedos do Pé
/
Vesícula
/
Extremidades
/
Pé
/
Membranas
Idioma:
En
Revista:
Annals of Dermatology
Ano de publicação:
2003
Tipo de documento:
Article