A case of Bart's syndrome / 대한피부과학회지
Korean Journal of Dermatology
;
: 620-623, 1993.
Artigo
em Coreano
| WPRIM
| ID: wpr-212079
ABSTRACT
Barts syndrome was desrribed by Bart(Bart et al, 1966) with hereditary congenital localized absence of skin from the lovrer legs associated with blistering of the sun and mouth and nail abnormalities. A newborn girl presented with a congenital localized absence of skn over both shins & dorsa of both feet which were covered with the thin, translucent, brown red glistening membranes. A number of blisters were seen on the back, thighs upper extremities, and both 2rd toe nails were absent. Electron microscopic examination of defected skin revealed dermo-epidermal . paration with focal disruption of basal lamina.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Pele
/
Coxa da Perna
/
Membrana Basal
/
Dedos do Pé
/
Sistema Solar
/
Vesícula
/
Extremidade Superior
/
Pé
/
Perna (Membro)
/
Membranas
Limite:
Feminino
/
Humanos
/
Recém-Nascido
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Ano de publicação:
1993
Tipo de documento:
Artigo
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