Boyd P A, Keeling J W
Department of Medical Genetics, Churchill Hospital, Headington, Oxford.
J Med Genet. 1992 Feb;29(2):91-7. doi: 10.1136/jmg.29.2.91.
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.
1983年至1988年间,对72例非免疫性水肿胎儿或新生儿进行了检查。最常见的关联是染色体异常;11例胎儿核型为45,X,11例为常染色体三体。另外20例根据尸检结果怀疑有染色体异常,但无法进行染色体培养或培养未成功。11例有感染的组织学证据;7例婴儿有主要结构异常,6例受影响胎儿为双胞胎。与1976年至1982年间检查的病例中8例(16%)相比,6例(8%)水肿病因未明确。与以前相比,水肿在胎儿存活时、妊娠20周前被诊断出的频率更高,且与染色体异常有关。