Literature DB >> 2606481

Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colli.

G Schwanitz1, K Zerres, U Gembruch, R Bald, M Hansmann.   

Abstract

Chromosome analyses were carried out in a series of 775 fetuses with morphological abnormalities diagnosed by ultrasound. Among these cases, 57 demonstrated non-immune hydrops fetalis with hygroma colli (group 1) and a further 116 non-immune hydrops fetalis without hygroma colli (group 2). Different chromosome abnormalities were found in 54.5% of cases of group 1 where chromosome analyses could be performed, and in 27.6% of cases of group 2. The most common aberrations were monosomy X and trisomy 21.

Entities:  

Mesh:

Year:  1989        PMID: 2606481     DOI: 10.1007/bf00210678

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  3 in total

1.  Nuchal cysts syndromes: etiology, pathogenesis, and prenatal diagnosis.

Authors:  B R Elejalde; M M de Elejalde; J Leno
Journal:  Am J Med Genet       Date:  1985-07

2.  Investigation of nonimmune hydrops fetalis.

Authors:  W Holzgreve; C J Curry; M S Golbus; P W Callen; R A Filly; J C Smith
Journal:  Am J Obstet Gynecol       Date:  1984-12-01       Impact factor: 8.661

3.  Hydrops fetalis and chromosomal trisomies.

Authors:  B G Landrum; D E Johnson; B Ferrara; S J Boros; T R Thompson
Journal:  Am J Obstet Gynecol       Date:  1986-05       Impact factor: 8.661

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.