Literature DB >> 24912022

Chorionic villus sampling for early prenatal diagnosis: Experience at a mainland Chinese hospital.

J Han1, M Pan, L Zhen, X Yang, Y-M Ou, C Liao, D-Z Li.   

Abstract

The aim of this study was to describe the experience of transabdominal chorionic villus sampling (CVS) at a mainland Chinese hospital. During a 7-year period, 1,172 pregnant women chose to have CVS for prenatal diagnosis. Details and outcome of all of these cases were reviewed. The median maternal age was 29 years (range 19-45). The median gestational age was 12 weeks (range 10-14). Fetal karyotyping and thalassaemia couples were the main indications (97.2%). Overall, 112 (9.7%) chromosomal abnormalities were identified. There were 91 (7.8%) major chromosomal abnormalities, including autosomal trisomy in 70 patients, sex chromosomal abnormalities in 17, triploidy in two and unbalanced chromosomal rearrangement abnormality in two. Additionally, 137 fetuses with severe thalassaemia syndrome were found, including 86 homozygous β-thalassaemia, and 51 homozygous α-thalassaemia or non-deletional haemoglobin H disease. The procedure failed to obtain an adequate sample in four (0.3%) patients. There were 229 pregnancies terminated for medical indications after CVS. There were three (0.3%) potentially procedure-related fetal losses. CVS is a safe and reliable prenatal diagnostic technique. It should be one of the options available to pregnant women who require prenatal diagnosis.

Entities:  

Keywords:  Chorionic villus sampling; fetal loss; prenatal diagnosis

Mesh:

Year:  2014        PMID: 24912022     DOI: 10.3109/01443615.2014.920793

Source DB:  PubMed          Journal:  J Obstet Gynaecol        ISSN: 0144-3615            Impact factor:   1.246


  3 in total

1.  Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping.

Authors:  Carlo Vermeulen; Geert Geeven; Elzo de Wit; Marjon J A M Verstegen; Rumo P M Jansen; Melissa van Kranenburg; Ewart de Bruijn; Sara L Pulit; Evelien Kruisselbrink; Zahra Shahsavari; Davood Omrani; Fatemeh Zeinali; Hossein Najmabadi; Theodora Katsila; Christina Vrettou; George P Patrinos; Joanne Traeger-Synodinos; Erik Splinter; Jeffrey M Beekman; Sima Kheradmand Kia; Gerard J Te Meerman; Hans Kristian Ploos van Amstel; Wouter de Laat
Journal:  Am J Hum Genet       Date:  2017-08-24       Impact factor: 11.025

2.  Noninvasive prenatal diagnosis of β-thalassemia by relative haplotype dosage without analyzing proband.

Authors:  Haoxian Li; Bole Du; Fuman Jiang; Yulai Guo; Yang Wang; Chunsheng Zhang; Xiaojing Zeng; Yuhuan Xie; Shuming Ouyang; Yexing Xian; Min Chen; Weiqiang Liu; Xiaofang Sun
Journal:  Mol Genet Genomic Med       Date:  2019-09-30       Impact factor: 2.183

3.  Prenatal Screening and Diagnosis of ß-Thalassemia in India: Is ARMS-PCR Enough?

Authors:  Shouriyo Ghosh; Sila Chakrabarti; Maitreyee Bhattacharyya
Journal:  Indian J Hematol Blood Transfus       Date:  2020-10-29       Impact factor: 0.915

  3 in total

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