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Fetal hepatosplenomegaly associated with transient myeloproliferative disorder in trisomy 21.

作者信息

Macones G A, Johnson A, Tilley D, Wade R, Wapner R

机构信息

Department of Obstetrics and Gynecology, Jefferson Medical College, Philadelphia, Pa., USA.

出版信息

Fetal Diagn Ther. 1995 Mar-Apr;10(2):131-3. doi: 10.1159/000264219.

Abstract

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/mm3 with a predominance of blast forms. In both cases the karyotype revealed trisomy 21.

摘要

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