CONGENITAL ANEMIA AND TRIPHALANGEAL THUMBS - A NEW SYNDROME

被引：86

作者：

AASE, JM

SMITH, DW

机构：

[1] University of Washington School of Medicine, Children's Orthopedic Hospital, Seattle, WA

来源：

JOURNAL OF PEDIATRICS | 1969年 / 74卷 / 03期

关键词：

D O I：

10.1016/S0022-3476(69)80208-8

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

A new syndrome of congenital hypoplastic anemia and triphalangeal thumbs has been found in two brothers, at least one of whom also has a congenital heart defect. It is not possible from the present data to discriminate between X-linked and autosomal recessive modes of inheritance. This condition is clearly distinguishable from Fanconi's fancytopenia, the radial aplasia-thrombocytopenia, and the Holt-Oram syndromes by physical and hematologic criteria. © 1969 The C. V. Mosby Company.

引用

页码：471 / &

共 4 条

[1] CONGENITAL (ERYTHROID) HYPOPLASTIC ANEMIA - A 25-YEAR STUDY [J].