Dystrophic Epidermolysis Bullosa in Two Sisters / 대한주산의학회잡지
Korean Journal of Perinatology
; : 485-489, 1999.
Article
ي Ko
| WPRIM
| ID: wpr-33772
المكتبة المسؤولة:
WPRO
ABSTRACT
Dystrophic epidermolysis bullosa is a rare, chronic non-inflammatory bullous disease, which easily forms bullae by minor mechanical trauma or spontaneously, is inherited either in an autosomal dominant or autosomal recessive fashion. We report herein two cases which presented with bullae, erosions and ulcers on extremities, buttock, chest, abdomen and face and loss of all nail since birth in two sisters. Bulla occured bencath the basal lamina histopathologically, anchoring fibrils were almost absent on electron miaoscopy in both cases. The two sisters represented dystrophic epidermolysis bullosa considering the absence of family history inheritcd in an autosomal dominant fashion and the clinical, histological and electronmicroscopic findings.
Key words
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Thorax
/
Ulcer
/
Basement Membrane
/
Buttocks
/
Epidermolysis Bullosa Dystrophica
/
Siblings
/
Parturition
/
Abdomen
/
Extremities
المحددات:
Humans
اللغة:
Ko
مجلة:
Korean Journal of Perinatology
السنة:
1999
نوع:
Article