DYSKERATOSIS-CONGENITA - CLINICAL AND GENETIC-HETEROGENEITY - REPORT OF A NEW CASE AND REVIEW OF THE LITERATURE

被引:0
作者
DRACHTMAN, RA
ALTER, BP
机构
[1] CUNY MT SINAI SCH MED, DEPT PEDIAT, DIV PEDIAT HEMATOL ONCOL, NEW YORK, NY 10029 USA
[2] CUNY MT SINAI SCH MED, POLLY ANNENBERG LEVEE HEMATOL CTR, DEPT MED, NEW YORK, NY 10029 USA
来源
AMERICAN JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 1992年 / 14卷 / 04期
关键词
DYSKERATOSIS; GENETICS; APLASTIC ANEMIA;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dyskeratosis congenita (DC) is a rare form of ectodermal dysplasia consisting of dystrophic nails, hyperpigmentation, and leukoplakia often associated with aplastic anemia. DC is considered to be an X-linked recessive trait, but affected females suggest genetic heterogeneity. We report an additional female with DC and review the world literature, indicating transmission in X-linked recessive, autosomal recessive, and autosomal dominant manners. The clinical and genetic aspects of DC are heterogeneous, and different patterns of inheritance are associated with distinct clinical manifestations. DC should be considered in the diagnosis of a patient with any features of the syndrome regardless of gender. Conversely, DC should be considered in patients with aplastic anemia at any age.
引用
收藏
页码:297 / 304
页数:8
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