A Case of Bart's Syndrome
Annals of Dermatology
;
: 23-26, 2003.
Article
Dans Anglais
| WPRIM
| ID: wpr-194040
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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Peau
/
Malformations
/
Orteils
/
Cloque
/
Membres
/
Pied
/
Membranes
langue:
Anglais
Texte intégral:
Annals of Dermatology
Année:
2003
Type:
Article
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