Literature DB >> 12752571

Evaluation of a Tay-Sachs disease screening program.

A A Gason1, E Sheffield, A Bankier, M A Aitken, S Metcalfe, K Barlow Stewart, M B Delatycki.   

Abstract

Tay-Sachs Disease (TSD) is an autosomal recessive neurodegenerative disorder. TSD is prevalent in the Ashkenazi Jewish population, and carrier screening programs have been implemented worldwide in these communities. A screening program initiated in 1997 involving the Melbourne Jewish community (Australia) incorporated education, counselling and carrier testing of high-school students aged 15 to 18 years. This study aimed to assess the participation rates, level of knowledge obtained and predicted feelings and attitudes of the students involved. Seven hundred and ten students participated, there was a 67% uptake for testing with a carrier rate of 1 in 28 determined. The level of knowledge of the students following education was high and of relative importance in regard to decision making, as were their feelings and attitudes about genetic testing for carrier status. A significant impediment to test uptake was the need for blood sampling, resulting in a recommendation for the introduction of DNA analysis on cheek brush samples. The evaluation of this program has given a wider scope for further development as well as providing valuable information for the implementation of community screening programs.

Entities:  

Mesh:

Year:  2003        PMID: 12752571     DOI: 10.1034/j.1399-0004.2003.00074.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  12 in total

1.  Carrier screening in preconception consultation in primary care.

Authors:  Sylvia A Metcalfe
Journal:  J Community Genet       Date:  2011-12-20

2.  Consumers' desire towards current and prospective reproductive genetic testing.

Authors:  Feighanne Hathaway; Esther Burns; Harry Ostrer
Journal:  J Genet Couns       Date:  2009-01-22       Impact factor: 2.537

3.  Community attitudes towards a Jewish community BRCA1/2 testing program.

Authors:  Nicole Cousens; Rajneesh Kaur; Bettina Meiser; Lesley Andrews
Journal:  Fam Cancer       Date:  2017-01       Impact factor: 2.375

4.  ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible.

Authors:  Martin B Delatycki; Michelle Wolthuizen; Veronica Collins; Elizabeth Varley; Joanna Craven; Katrina J Allen; Lyle C Gurrin; Maryanne Aitken; M Kaye Trembath; Lyndal Bond; Gabrielle R Wilson; Sarah E M Stephenson; Ivan Macciocca; Chriselle Hickerton; Paul J Lockhart; Sylvia A Metcalfe
Journal:  Eur J Hum Genet       Date:  2012-01-11       Impact factor: 4.246

5.  Using the impact of event scale to evaluate psychological response to being a phenylketonuria gene carrier.

Authors:  Catherine Y Read
Journal:  J Genet Couns       Date:  2004-06       Impact factor: 2.537

6.  "He didn't say that thalassaemia might come up" - β-thalassaemia carriers' experiences and attitudes.

Authors:  Nicole E Cousens; Clara L Gaff; Sylvia A Metcalfe; Martin B Delatycki
Journal:  J Community Genet       Date:  2013-01-13

Review 7.  Population programs for the detection of couples at risk for severe monogenic genetic diseases.

Authors:  Joël Zlotogora
Journal:  Hum Genet       Date:  2009-04-24       Impact factor: 4.132

8.  High school Tay-Sachs disease carrier screening: 5 to 11-year follow-up.

Authors:  Helen Curd; Sharon Lewis; Ivan Macciocca; Margaret Sahhar; Vicki Petrou; Agnes Bankier; Sari Lieberman; Ephrat Levy-Lahad; Martin B Delatycki
Journal:  J Community Genet       Date:  2013-07-27

Review 9.  Tay-Sachs disease: current perspectives from Australia.

Authors:  Raelia M Lew; Leslie Burnett; Anné L Proos; Martin B Delatycki
Journal:  Appl Clin Genet       Date:  2015-01-21

10.  Knowledge and attitudes toward a free education and Ashkenazi Jewish carrier testing program.

Authors:  G Hegwer; C Fairley; J Charrow; K E Ormond
Journal:  J Genet Couns       Date:  2006-02       Impact factor: 2.717

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.