A Case of Epidermolysis Bullosa Dystrophica / 대한피부과학회지
Korean Journal of Dermatology
;
: 387-391, 1985.
Artículo
en Coreano
| 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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Piel
/
Dedos del Pie
/
Epidermólisis Ampollosa Distrófica
/
Vesícula
/
Epidermólisis Ampollosa
/
Cicatriz
/
Sindactilia
/
Parto
/
Dedos
/
Pie
Límite:
Child, preschool
/
Femenino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Año:
1985
Tipo del documento:
Artículo
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