Literature DB >> 14501833

Screening for Fragile X Syndrome: parent attitudes and perspectives.

Debra Skinner1, Karen L Sparkman, Donald B Bailey.   

Abstract

PURPOSE: This study examined the attitudes and beliefs of 442 parents of children with fragile X syndrome (FXS) regarding different screening options for FXS.
METHODS: A survey was administered to parents of children with FXS across the U.S.
RESULTS: Parents indicated their support for voluntary screening for FXS, especially carrier and newborn screening. They also thought advantages of widespread screening to be more likely than disadvantages.
CONCLUSION: Parents' support for FXS screening is at odds with current screening criteria, but as new genetic knowledge and technologies reconfigure these criteria, it will be important to take parents' perspectives into account.

Entities:  

Keywords:  Empirical Approach; Genetics and Reproduction

Mesh:

Year:  2003        PMID: 14501833     DOI: 10.1097/01.gim.0000086480.69309.1e

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  24 in total

1.  "This lifetime commitment": Public conceptions of disability and noninvasive prenatal genetic screening.

Authors:  Rosemary J Steinbach; Megan Allyse; Marsha Michie; Emily Y Liu; Mildred K Cho
Journal:  Am J Med Genet A       Date:  2015-11-14       Impact factor: 2.802

2.  "It gives them more options": preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare.

Authors:  Alison D Archibald; Chriselle L Hickerton; Samantha A Wake; Alice M Jaques; Jonathan Cohen; Sylvia A Metcalfe
Journal:  J Community Genet       Date:  2016-02-03

3.  "If He Has it, We Know What to Do": Parent Perspectives on Familial Risk for Autism Spectrum Disorder.

Authors:  Katherine E MacDuffie; Lauren Turner-Brown; Annette M Estes; Benjamin S Wilfond; Stephen R Dager; Juhi Pandey; Lonnie Zwaigenbaum; Kelly N Botteron; John R Pruett; Joseph Piven; Holly L Peay
Journal:  J Pediatr Psychol       Date:  2020-03-01

4.  Screening for lysosomal storage disorders--a clinical perspective.

Authors:  Janice M Fletcher
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       Impact factor: 4.982

5.  Parents' decisions to screen newborns for FMR1 gene expansions in a pilot research project.

Authors:  Debra Skinner; Summer Choudhury; John Sideris; Sonia Guarda; Allen Buansi; Myra Roche; Cynthia Powell; Donald B Bailey
Journal:  Pediatrics       Date:  2011-05-29       Impact factor: 7.124

6.  Genetic knowledge and attitudes of parents of children with congenital heart defects.

Authors:  Sara M Fitzgerald-Butt; Jennifer Klima; Kelly Kelleher; Deena Chisolm; Kim L McBride
Journal:  Am J Med Genet A       Date:  2014-09-24       Impact factor: 2.802

7.  Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors.

Authors:  Allyn McConkie-Rosell; Brenda Finucane; Amy Cronister; Liane Abrams; Robin L Bennett; Barbara J Pettersen
Journal:  J Genet Couns       Date:  2005-08       Impact factor: 2.537

8.  Fragile X screening: attitudes of genetic health professionals.

Authors:  Kruti Acharya; Lainie Friedman Ross
Journal:  Am J Med Genet A       Date:  2009-02-15       Impact factor: 2.802

9.  Prenatal screening for fragile x: carriers, controversies, and counseling.

Authors:  Julie F Gutiérrez; Komal Bajaj; Susan D Klugman
Journal:  Rev Obstet Gynecol       Date:  2013

10.  Decisions about testing and termination of pregnancy for different fetal conditions: a qualitative study of European White and Pakistani mothers of affected children.

Authors:  Shenaz Ahmed; Jenny Hewison; Josephine M Green; Howard S Cuckle; Janet Hirst; Jim G Thornton
Journal:  J Genet Couns       Date:  2008-10-09       Impact factor: 2.537

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