Literature DB >> 3588542

Parental decisions regarding termination of pregnancy following prenatal detection of sex chromosome abnormality.

M Holmes-Siedle, M Ryynanen, R H Lindenbaum.   

Abstract

In the period of a retrospective study (1970-1984 inclusive) forty cases of sex chromosome aneuploidy were identified at amniocentesis in Oxford, England and in Kuopio, Finland; 25 of these pregnancies were subsequently terminated. A decision to continue was made more often for XYY and XXX karyotypes, by older mothers and older fathers, by couples with more previous children, and by couples living in England. A decision to terminate was made more often for XXY and non-mosaic 45,X karyotypes, by younger mothers and younger fathers, by couples with few previous children, in all cases with abnormal ultrasound findings, when post-amniocentesis counselling was given by an obstetrician, and by couples living in Finland. Previous miscarriages, or terminations of pregnancy, previous problems with infertility, marital status, or the type of counselling given before amniocentesis, appeared not to influence a couples' decision. Religious and ethical ideas were not studied systematically at the time and cannot be reported on.

Entities:  

Mesh:

Year:  1987        PMID: 3588542     DOI: 10.1002/pd.1970070403

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


  10 in total

1.  Experiences of prenatal diagnosis of spina bifida or hydrocephalus in parents who decide to continue with their pregnancy.

Authors:  Julie Chaplin; Robert Schweitzer; Shelley Perkoulidis
Journal:  J Genet Couns       Date:  2005-04       Impact factor: 2.537

2.  Variables influencing pregnancy termination following prenatal diagnosis of fetal chromosome abnormalities.

Authors:  Anne Hawkins; Ana Stenzel; Joanne Taylor; Valerie Y Chock; Louanne Hudgins
Journal:  J Genet Couns       Date:  2012-09-23       Impact factor: 2.537

3.  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

4.  Parental decisions regarding a prenatally detected fetal chromosomal abnormality and the impact of genetic counseling: an analysis of 38 cases with aneuploidy in Southeast Turkey.

Authors:  Mahmut Balkan; Sevgi Kalkanli; Halit Akbas; Ahmet Yalinkaya; M Nail Alp; Turgay Budak
Journal:  J Genet Couns       Date:  2010-01-30       Impact factor: 2.537

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

Review 6.  Ethical considerations in prenatal diagnosis.

Authors:  E A Gates
Journal:  West J Med       Date:  1993-09

7.  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

8.  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

9.  Pregnant women's views on how to promote the use of a decision aid for Down syndrome prenatal screening: a theory-informed qualitative study.

Authors:  Titilayo Tatiana Agbadjé; Matthew Menear; Michèle Dugas; Marie-Pierre Gagnon; Samira Abbasgholizadeh Rahimi; Hubert Robitaille; Anik M C Giguère; François Rousseau; Brenda J Wilson; France Légaré
Journal:  BMC Health Serv Res       Date:  2018-06-08       Impact factor: 2.655

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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