Literature DB >> 8117059

Chromosomal findings in fetuses with ultrasonographically diagnosed ventriculomegaly.

G Schwanitz1, H Schüler, U Gembruch, K Zerres.   

Abstract

Out of 1101 fetuses with prenatally diagnosed malformations and/or growth retardation 166 (15.1%) revealed a ventriculomegaly. Out of these 18 fetuses (10.8%) demonstrated a chromosomal disorder. Within the group of 97 fetuses with isolated hydrocephalus 6 (6.2%) revealed a chromosomal abnormality. Two fetuses among 29 (6.9%) with hydrocephalus and spina bifida as the only additional sign showed pathologic karyotypes. Among fetuses with additional malformations, 10 out of 40 (25.0%) had a chromosomal disorder. Our data demonstrate that a prenatally diagnosed hydrocephalus should be regarded as an indication for a chromosomal analysis, with the highest amount of chromosomal disorders in fetuses with different additional malformations.

Entities:  

Mesh:

Year:  1993        PMID: 8117059

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  2 in total

1.  Pathological approach to the diagnosis of hydrocephalus.

Authors:  M V Squier
Journal:  J Clin Pathol       Date:  1997-03       Impact factor: 3.411

2.  Approach to the sonographic evaluation of fetal ventriculomegaly at 11 to 14 weeks gestation.

Authors:  Gwendolin Manegold-Brauer; Anton Oseledchyk; Anne Floeck; Christoph Berg; Ulrich Gembruch; Annegret Geipel
Journal:  BMC Pregnancy Childbirth       Date:  2016-01-12       Impact factor: 3.007

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.