Prenatally diagnosed fetal ventriculomegaly; Prognosis and outcome

被引:1
作者
Den Hollander, NS
Vinkesteijn, A
Schmitz-Van Splunder, P
Catsman-Berrevoets, CE
Wladimiroff, JW
机构
[1] Erasmus Univ, Acad Hosp Rotterdam Dijkzigt, Dept Obstet & Gynaecol, Sophia Childrens Hosp, NL-3015 GD Rotterdam, Netherlands
[2] Erasmus Univ, Acad Hosp Rotterdam Dijkzigt, Dept Child Neurol, Sophia Childrens Hosp, NL-3015 GD Rotterdam, Netherlands
关键词
ventriculomegaly; psycho-motor development;
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The purpose of the present study was to determine the postnatal outcome and prognostic factors of prenatally diagnosed ventriculomegaly, and to establish the relationship between prenatal sonographic measurements and postnatal psychomotor development. A total of 42 singleton pregnancies with sonographically determined fetal ventriculomegaly at 20-38 weeks' gestation were reviewed, together with follow-up data on postnatal outcome at a mean of 29 months after delivery. Sonographic measurements included head circumference, cerebral lateral ventricular diameter at the anterior and posterior horn level, and hemisphere diameter. Classification of psyche-motor development consisted of assessment of motoric behaviour, speech, communication and social skills ('Van Wiechen' classification). Perinatal mortality rate was 38 per cent, of which half were directly associated with cephalocentesis. Only the ventricle/hemisphere ratio for the anterior and posterior horn of the lateral cerebral ventricles was significantly higher among perinatal deaths than amongst the survivors. Within the subset of survivors (n=26), psyche-motor development was normal in 46 per cent. Postnatal examination revealed syndromal anomalies in five infants, of which four were associated with psyche-motor retardation. Prenatally diagnosed ventriculomegaly has a poor postnatal outcome with more than 50 per cent of the live-born infants demonstrating abnormal psyche-motor development. The predictive value of fetal biometric measurements is poor. The presence of syndromal anomalies emphasizes the need for genetic counselling in future pregnancies. (C) 1998 John Wiley & Sons, Ltd.
引用
收藏
页码:557 / 566
页数:10
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