Literature DB >> 2624268

Decisions following the intrauterine diagnosis of sex chromosome aneuploidy.

A Robinson1, B G Bender, M G Linden.   

Abstract

This is a report of 327 phone calls to our center concerning the intrauterine diagnosis of sex chromosome abnormalities (SCA). The first author (A.R.) responded to each by counseling either the parents or the referring professional. Sixty-two percent continued the pregnancy. When the parents were counseled directly, the percentage continuing the pregnancy was significantly higher than when the information was transmitted through the professionals. Our results are different from most reports in these situations, and suggest that well-informed couples, counseled by geneticists, are more likely to continue these pregnancies. The possible occurrence of SCA should be considered in preamniocentesis counseling.

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Year:  1989        PMID: 2624268     DOI: 10.1002/ajmg.1320340420

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  10 in total

Review 1.  Triple X syndrome: a review of the literature.

Authors:  Maarten Otter; Constance T R M Schrander-Stumpel; Leopold M G Curfs
Journal:  Eur J Hum Genet       Date:  2009-07-01       Impact factor: 4.246

2.  Continuation of Pregnancy Following the Diagnosis of a Fetal Sex Chromosome Abnormality: A Study of Parents' Counseling Needs and Experiences.

Authors:  N Petrucelli; M Walker; E Schorry
Journal:  J Genet Couns       Date:  1998-10       Impact factor: 2.537

3.  How do obstetric providers discuss referrals for prenatal genetic counseling?

Authors:  Barbara A Bernhardt; Carrie Mastromarino Haunstetter; Debra Roter; Gail Geller
Journal:  J Genet Couns       Date:  2005-04       Impact factor: 2.537

4.  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

Review 5.  Maternal serum screening for neural tube defects and fetal chromosome abnormalities.

Authors:  N C Rose; M T Mennuti
Journal:  West J Med       Date:  1993-09

6.  Counselling following diagnosis of a fetal abnormality: the differing approaches of obstetricians, clinical geneticists, and genetic nurses.

Authors:  T Marteau; H Drake; M Bobrow
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

7.  Children with sex chromosome trisomies: parental disclosure of genetic status.

Authors:  Nikki C Gratton; Jessica Myring; Prisca Middlemiss; Deborah Shears; Diana Wellesley; Sarah Wynn; Dorothy Vm Bishop; Gaia Scerif
Journal:  Eur J Hum Genet       Date:  2015-08-26       Impact factor: 4.246

8.  Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child.

Authors:  Kirsten A Riggan; Sharron Close; Megan A Allyse
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-03-17       Impact factor: 3.908

9.  Offering antenatal sickle cell and thalassaemia screening to pregnant women in primary care: a qualitative study of women's experiences and expectations of participation.

Authors:  Vicki Tsianakas; Karl Atkin; Michael W Calnan; Elizabeth Dormandy; Theresa M Marteau
Journal:  Health Expect       Date:  2011-03-03       Impact factor: 3.377

10.  Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who?

Authors:  L Aliberti; I Gagliardi; S Bigoni; S Lupo; S Caracciolo; A Ferlini; A M Isidori; M C Zatelli; M R Ambrosio
Journal:  J Community Genet       Date:  2022-03-05
  10 in total

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