Literature DB >> 9492519

Prenatal diagnosis of Down syndrome: mothers' reflections on supports needed from diagnosis to birth.

D T Helm1, S Miranda, N A Chedd.   

Abstract

A qualitative study involving 10 mothers who received a prenatal diagnosis of Down syndrome and chose to continue their pregnancy was presented. The time frame considered was diagnosis to delivery. We looked at how the diagnosis was presented, the decision to continue the pregnancy, and the mothers' experience with professionals from diagnosis to delivery. Mothers' suggestions to others facing the same challenges and to their health care providers were discussed as were the types of support given these mothers and what was or would have been most helpful to them. The importance of professionals reviewing their procedures and protocols for working with families facing similar circumstances was stressed.

Mesh:

Year:  1998        PMID: 9492519     DOI: 10.1352/0047-6765(1998)036<0055:PDODSM>2.0.CO;2

Source DB:  PubMed          Journal:  Ment Retard        ISSN: 0047-6765


  11 in total

1.  Exploring adoption with clients: the need for adoption education within the genetic counseling profession.

Authors:  Cassandra L Perry; Martha J Henry
Journal:  J Genet Couns       Date:  2010-03-16       Impact factor: 2.537

2.  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

3.  Practice guidelines for communicating a prenatal or postnatal diagnosis of Down syndrome: recommendations of the national society of genetic counselors.

Authors:  Kathryn B Sheets; Blythe G Crissman; Cori D Feist; Susan L Sell; Lisa R Johnson; Kelly C Donahue; Diane Masser-Frye; Gail S Brookshire; Amanda M Carre; Danielle Lagrave; Campbell K Brasington
Journal:  J Genet Couns       Date:  2011-05-27       Impact factor: 2.537

4.  Cell-free fetal DNA testing for fetal aneuploidy and beyond: clinical integration challenges in the US context.

Authors:  Megan Allyse; Lauren C Sayres; Jaime S King; Mary E Norton; Mildred K Cho
Journal:  Hum Reprod       Date:  2012-08-03       Impact factor: 6.918

Review 5.  The relationship between the genetic counseling profession and the disability community: a commentary.

Authors:  Anne C Madeo; Barbara B Biesecker; Campbell Brasington; Lori H Erby; Kathryn F Peters
Journal:  Am J Med Genet A       Date:  2011-05-12       Impact factor: 2.802

6.  What Predicts the Use of Genetic Counseling Services After the Birth of a Child with Down Syndrome?

Authors:  Veronica Collins; Jane Halliday; Robert Williamson
Journal:  J Genet Couns       Date:  2003-02       Impact factor: 2.537

7.  What is a "balanced" description? Insight from parents of individuals with down syndrome.

Authors:  Catriona Hippman; Angela Inglis; Jehannine Austin
Journal:  J Genet Couns       Date:  2011-12-20       Impact factor: 2.537

Review 8.  A systematic review of decision support needs of parents making child health decisions.

Authors:  Cath Jackson; Francine M Cheater; Innes Reid
Journal:  Health Expect       Date:  2008-09       Impact factor: 3.377

9.  Is preparation a good reason for prenatal genetic testing? Ethical and critical questions.

Authors:  Marsha Michie
Journal:  Birth Defects Res       Date:  2020-03-01       Impact factor: 2.344

10.  Should We Genetically Select for the Beauty Norm of Fair Skin?

Authors:  Herjeet Marway
Journal:  Health Care Anal       Date:  2018-09
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