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胎儿水肿

Fetal hydrops.

作者信息

Boyd P A, Keeling J W

机构信息

Department of Medical Genetics, Churchill Hospital, Headington, Oxford.

出版信息

J Med Genet. 1992 Feb;29(2):91-7. doi: 10.1136/jmg.29.2.91.

Abstract

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.

摘要

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。

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本文引用的文献

3
The obstetric management of non-immunological hydrops.非免疫性水肿的产科处理
Br J Obstet Gynaecol. 1986 Mar;93(3):226-34. doi: 10.1111/j.1471-0528.1986.tb07898.x.
7
Intrauterine treatment of idiopathic hydrops fetalis.胎儿特发性水肿的宫内治疗。
J Perinat Med. 1988;16(2):133-8. doi: 10.1515/jpme.1988.16.2.133.
10
Cardiac abnormalities and nonimmune hydrops fetalis: a coincidental, not causal, relationship.
Pediatr Pathol. 1989;9(1):11-7. doi: 10.3109/15513818909022328.

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