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Dominant dystrophic epidermolysis bullosa of Cockayne-Touraine in father and son: clinical and ultrastructural similarities.

作者信息

De Raeve L, De Dobbeleer G, Song M, Achten G

机构信息

Department of Dermatology, Université Libre de Bruxelles, Belgium.

出版信息

Dermatologica. 1988;176(2):91-4. doi: 10.1159/000248678.

DOI:10.1159/000248678
PMID:3371524
Abstract

Dominant dystrophic epidermolysis bullosa of Cockayne-Touraine occurred in a father and his son. Clinically, the child presented evident blistering, while the father, despite of his work, where minimal skin traumata frequently occur, was rarely affected. Absent or rudimentary anchoring fibrils were seen in the normal-appearing skin of the father; this suggests that other factors may play a role in the dermolytic separation.

摘要

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Dominant dystrophic epidermolysis bullosa of Cockayne-Touraine in father and son: clinical and ultrastructural similarities.
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2
Ultrastructural studies in epidermolysis bullosa hereditaria. II. Dominant dystrophic type of Cockayne and Touraine.遗传性大疱性表皮松解症的超微结构研究。II. 科凯恩和图赖讷显性营养不良型
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The Cockayne-Touraine type of dominant dystrophic epidermolysis bullosa--ultrastructural similarities to the Pasini variant.科凯恩-图赖讷型显性营养不良性大疱性表皮松解症——与帕西尼变异型的超微结构相似性。
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