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A Case of Epidermolysis Bullosa Hereditaria

Journal of the Korean Pediatric Society 1974;17(2):168-171.
Published online February 28, 1974.
A Case of Epidermolysis Bullosa Hereditaria
Myung Suk Kim1, Young Soon Lee1, Sung Kyu Lee1, Duk Jin Yun1, Chung Koo Cho2, In Joon Choi3
1Department of Pediatrics, Yonsei University College of Medicine Seoul、Korea
2Department of Dermatology, Yonsei University College of Medicine Seoul、Korea
3Department of Pathology, Yonsei University College of Medicine Seoul、Korea
선천성 표피수포증 1 예
김명숙1, 이영순1, 이승규1, 윤덕진1, 조정구2, 최인준3
1연세대학교 의과대학 소아과학교실
2연세대학교 의과대학피부과학교실
3연세대학교 의과대학병리학교실
Abstract
Epidermolysis bullosa hereditaria is an uncommon skin disease which is manifest at birth or in infancy. It is characterized by blister formation occuring spontaneously or after friction or slight trauma. Recently, we experienced a case of epidermolysis bullosa hereditaria in one day old newborn infant, who was developed bullae on the neck, abdomen, both extremities and buttock. A brief review of literature was made.


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