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Bart 증후군 1예

Other Titles
 A Case of Bart`s Syndrome 
Authors
 이규엽  ;  류동진  ;  정혜진  ;  방동식 
Citation
 Korean Journal of Dermatology (대한피부과학회지), Vol.47(4) : 463-467, 2009 
Journal Title
 Korean Journal of Dermatology (대한피부과학회지) 
ISSN
 4944-4739 
Issue Date
2009
Keywords
Aplasia cutis congenita ; Bart’s syndrome ; Epidermolysis bullosa
Abstract
Aplasia cutis congenita is a rare congenital skin defect that presents with sharply outlined ulcerations. The most common site of this disease is the scalp, yet when other areas of the body are involved, there is higher incidence of concomitant congenital diseases or malformations. Bart`s syndrome is a rare inherited condition with congenital skin defects that are associated with epidermolysis bullosa. An infant presented with congenital skin defects on the leg, and the infant had recurrent bullous skin lesions on the both hands, feet, wrists and ankles. The skin defect caused only small scar formation and no handicap regarding function and appearance, yet continuously new bullous lesion developed and healed on the both distal extremities. He was diagnosed as suffering with epidermolysis bullosa with the histological findings of epidermal cleavage and negative direct immunofluorescence findings. Herein, we report on a case of Bart`s syndrome that displayed aplasia cutis congenita over the lower extremities and skin blistering.
Files in This Item:
T200901045.pdf Download
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
Yonsei Authors
Bang, Dong Sik(방동식)
Chung, Hye Jin(정혜진)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/103772
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