FETAL HEPATOSPLENOMEGALY ASSOCIATED WITH TRANSIENT MYELOPROLIFERATIVE DISORDER IN TRISOMY-21

被引：24

作者：

MACONES, GA ^{[1
]}

JOHNSON, A ^{[1
]}

TILLEY, D ^{[1
]}

WADE, R ^{[1
]}

WAPNER, R ^{[1
]}

机构：

[1] JEFFERSON MED COLL,DEPT OBSTET & GYNECOL,DIV MATERNAL FETAL MED,PHILADELPHIA,PA

来源：

FETAL DIAGNOSIS AND THERAPY | 1995年 / 10卷 / 02期

关键词：

DOWN SYNDROME; HEPATOSPLENOMEGALY;

D O I：

10.1159/000264219

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

The in utero diagnosis of fetal myeloproliferative disease was made by cordocentesis following the ultrasound appearance of fetal hepatosplenomegaly and mild hydrops. The 2 fetuses reported both had leukocyte counts greater than 75,000/mm(3) with a predominance of blast forms. In both cases the karyotype revealed trisomy 21.

引用

页码：131 / 133

页数：3

共 7 条

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