Literature DB >> 10701849

Parental decisions following prenatal diagnosis of sex chromosome aneuploidy: a trend over time.

S M Christian1, D Koehn, R Pillay, A MacDougall, R D Wilson.   

Abstract

Research over the last 20 years has considerably changed the understanding of the natural history and prognosis for individuals with a diagnosis of sex chromosome aneuploidy (SCA). A cross-sectional retrospective analysis of factors influencing parental decisions following a prenatal diagnosis of SCA during the time period of 1971-97 was performed. The records of 169 fetuses with a prenatal karyotype of 45,X, 47,XXX, 47,XXY, and 47,XYY were reviewed. Mosaic karyotypes for SCA were also included. Information reviewed involved: parental decision, the type of SCA, the presence or absence of mosaicism, the presence or absence of a fetal anomaly diagnosed by ultrasound examination, indication for prenatal diagnosis, prenatal procedure performed, parental age, marital status, previous pregnancy history, family history, ethnicity, religion, education, and profession. A significant correlation was found between the decision to continue a pregnancy and the type of SCA and the presence of fetal abnormalities on ultrasound examination. In addition, this study examined differences in parental decisions over time for the years in question. A statistically significant trend was observed with a higher rate of pregnancy continuation in the more recent years.

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Year:  2000        PMID: 10701849

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  7 in total

1.  Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.

Authors:  Faustina Lalatta; Donatella Quagliarini; Emanuela Folliero; Ugo Cavallari; Barbara Gentilin; Pierangela Castorina; Francesca Forzano; Serena Forzano; Enrico Grosso; Valeria Viassolo; Valeria Giorgia Naretto; Stefania Gattone; Florinda Ceriani; Francesca Faravelli; Luigi Gargantini
Journal:  Eur J Pediatr       Date:  2010-05-15       Impact factor: 3.183

2.  What parents are told after prenatal diagnosis of a sex chromosome abnormality: interview and questionnaire study.

Authors:  L Abramsky; S Hall; J Levitan; T M Marteau
Journal:  BMJ       Date:  2001-02-24

3.  Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2019-02-19

4.  Prenatal Diagnosis of Chromosome Abnormalities: A 13-Year Institution Experience.

Authors:  Carmen Comas; Mónica Echevarria; María Ángeles Rodríguez; Ignacio Rodríguez; Bernat Serra; Vincenzo Cirigliano
Journal:  Diagnostics (Basel)       Date:  2012-11-19

5.  Lack of consensus in the choice of termination of pregnancy for Turner syndrome in France.

Authors:  Monika Hermann; Babak Khoshnood; Olivia Anselem; Claire Bouvattier; Aurélie Coussement; Sophie Brisset; Alexandra Benachi; Vassilis Tsatsaris
Journal:  BMC Health Serv Res       Date:  2019-12-23       Impact factor: 2.655

6.  Positive predictive value of noninvasive prenatal testing for sex chromosome abnormalities.

Authors:  Nan Guo; Meiying Cai; Min Lin; Huili Xue; Hailong Huang; Liangpu Xu
Journal:  Mol Biol Rep       Date:  2022-08-12       Impact factor: 2.742

Review 7.  Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis.

Authors:  Lauren Westerfield; Sandra Darilek; Ignatia B van den Veyver
Journal:  J Clin Med       Date:  2014-09-12       Impact factor: 4.241

  7 in total

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