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.
| Original language | English |
|---|---|
| Pages (from-to) | 131-133 |
| Number of pages | 3 |
| Journal | Fetal Diagnosis and Therapy |
| Volume | 10 |
| Issue number | 2 |
| DOIs | |
| State | Published - 1995 |
Keywords
- Down syndrome
- Hepatosplenomegaly