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.
|Number of pages||3|
|Journal||Fetal Diagnosis and Therapy|
|State||Published - 1995|
- Down syndrome