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

页码：332 / 334

页数：3

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