Fetal Hepatosplenomegaly Associated with Transient Myeloproliferative Disorder in Trisomy 21
- 1 January 1995
- journal article
- case report
- Published by S. Karger AG in Fetal Diagnosis and Therapy
- Vol. 10 (2) , 131-133
- https://doi.org/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.Keywords
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