Mild fetal lateral cerebral ventriculomegaly: clinical course and outcome.

摘要: The neonatal, pathologic outcome and karyotypic abnormalities are reported for 44 fetuses with mild ventriculomegaly diagnosed antenatally. Seventeen of these (39%) had other ultrasonographic defects, five (12%) abnormal karyotypes. Five pregnancies were electively aborted three died in the neonatal period. Twenty-six (72%) remaining 36 live-born neonates developmentally clinically normal at 3 to 18 months age. Twenty-one 26 isolated as only finding. 10 infants impaired, prenatal abnormality. In conclusion, data show that have a lower incidence associated anomalies better than more severe ventricular dilatation, literature. majority an finding karyotype developing normally.