Dyskeratosis congenita

被引：0
|
作者：
Caux, F
Aractingi, S
Sawaf, MH
Ouhayoun, JP
Dubertret, L
Gluckman, E
机构：
[1] HOP ST LOUIS,SERV DERMATOL,F-75475 PARIS,FRANCE
[2] INST BIOMED CORDELIERS,LAB ODONTOL,PARIS,FRANCE
[3] HOP ST LOUIS,SERV GREFFES MOELLE,PARIS,FRANCE
来源：
EUROPEAN JOURNAL OF DERMATOLOGY | 1996年 / 6卷 / 05期
关键词：
dyskeratosis congenita; leukoplakia; nail dystrophy; pigmentary changes; bone marrow aplasia;
D O I：
暂无
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
Dyskeratosis congenita is a rare, usually X-linked disorder typically characterized by leucokeratosis of the mucous membranes, nail dystrophy, reticulate hyperpigmentation and progressive bone marrow aplasia. We report a new case of a male patient with characteristic muco-cutaneous changes and bone marrow aplasia. We discuss the pathogenesis of this disease which remains unexplained.
引用
收藏
页码：332 / 334
页数：3
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