A Case of Epidermolysis Bullosa Dystrophica / 대한피부과학회지
Korean Journal of Dermatology
;
: 387-391, 1985.
Article
Dans Coréen
| WPRIM
| ID: wpr-106116
ABSTRACT
Epidermolysis bullosa dystrophica(EBD) is a rare, hereditary and chronic mechanobullous disease characterized by blistering and erosions of the skin in response to even minor trauma. A 5-year old girl visited with a complaint of continuous vesicobullous skin eruptions since birth. On examination, bullae, vesicles, atrophic scars, crusts and eroions were scattered on whole body. Loss of finger and toe nails, partial syndactyly of all toe webs and milia on dorsa of feet were noticed. We present a case of EBD that seems to be a recessive type considering the absence of family history with histopathologic and electron microscopic findings.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Peau
/
Orteils
/
Épidermolyse bulleuse dystrophique
/
Cloque
/
Épidermolyse bulleuse
/
Cicatrice
/
Syndactylie
/
Parturition
/
Doigts
/
Pied
Limites du sujet:
Enfant d'âge préscolaire
/
Femelle
/
Humains
langue:
Coréen
Texte intégral:
Korean Journal of Dermatology
Année:
1985
Type:
Article
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