FETAL HYDROPS

被引:29
作者
BOYD, PA [1 ]
KEELING, JW [1 ]
机构
[1] JOHN RADCLIFFE HOSP,DEPT PAEDIAT PATHOL,OXFORD OX3 9DU,ENGLAND
关键词
D O I
10.1136/jmg.29.2.91
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Seventy-two fetuses or neonates with non-immune hydrops were examined between 1983 and 1988. The commonest association was chromosome abnormality; 11 fetuses had a 45, X karyotype and 11 autosomal trisomy. Chromosome abnormality was suspected in a further 20 on necropsy findings but chromosome culture was not possible or unsuccessful. In 11 cases there was histological evidence of infection; seven babies had major structural anomalies and six affected fetuses were twins. In six (8%) the cause of hydrops was not determined compared with eight (16%) of cases examined between 1976 and 1982. Hydrops was diagnosed more frequently while the fetus was alive, before 20 weeks' gestation, and associated with chromosome anomaly than found previously.
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页码:91 / 97
页数:7
相关论文
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