Literature DB >> 11142756

Tay-Sachs disease carrier screening: a 21-year experience.

G D'Souza1, C L McCann, J Hedrick, C Fairley, H L Nagel, J D Kushner, R Kessel.   

Abstract

This paper presents the findings of a community-based carrier screening program for Tay-Sachs disease, initiated on the University of Wisconsin-Madison campus in 1978. The Madison Community Tay-Sachs Screening Program (MCTSSP) is a collaborative, interdisciplinary program that organizes and conducts periodic screening for Tay-Sachs disease (TSD) for the purpose of identifying Tay-Sachs carriers. We present and analyze data on carrier detection with regard to various demographics, including family history of TSD, ancestry, gender, medication exposure, and illness. Individuals participating in the MCTSSP between 1978 and 1999 were primarily of the target population, and the carrier rate was within the expected range (1/25). Despite aggressive publicity efforts and a well-established program, attendance at the screens has declined. A recent survey of Jewish undergraduate students at the University of Wisconsin-Madison showed poor recall of family screen history and carrier status and reinforced the perception that utilization of the Madison screening program has been low. Ways to increase awareness of and interest in carrier screening for TSD are explored.

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Year:  2000        PMID: 11142756     DOI: 10.1089/10906570050501470

Source DB:  PubMed          Journal:  Genet Test        ISSN: 1090-6576


  7 in total

1.  Towards quality assurance in the determination of lysosomal enzymes: a two-centre study.

Authors:  Z Lukacs; A Keil; V Peters; A Kohlschütter; G F Hoffmann; M Cantz; J Kopitz
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

2.  Carrier testing for severe childhood recessive diseases by next-generation sequencing.

Authors:  Callum J Bell; Darrell L Dinwiddie; Neil A Miller; Shannon L Hateley; Elena E Ganusova; Joann Mudge; Ray J Langley; Lu Zhang; Clarence C Lee; Faye D Schilkey; Vrunda Sheth; Jimmy E Woodward; Heather E Peckham; Gary P Schroth; Ryan W Kim; Stephen F Kingsmore
Journal:  Sci Transl Med       Date:  2011-01-12       Impact factor: 17.956

3.  Comprehensive carrier screening and molecular diagnostic testing for recessive childhood diseases.

Authors:  Stephen Kingsmore
Journal:  PLoS Curr       Date:  2012-05-02

Review 4.  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

5.  Screening for Tay-Sachs disease carriers by full-exon sequencing with novel variant interpretation outperforms enzyme testing in a pan-ethnic cohort.

Authors:  Alana C Cecchi; Elizabeth S Vengoechea; Kristjan E Kaseniit; Melanie W Hardy; Laura A Kiger; Nikita Mehta; Imran S Haque; Krista Moyer; Patricia Z Page; Dale Muzzey; Karen A Grinzaid
Journal:  Mol Genet Genomic Med       Date:  2019-07-10       Impact factor: 2.183

6.  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

7.  Next-generation DNA sequencing of HEXA: a step in the right direction for carrier screening.

Authors:  Jodi D Hoffman; Valerie Greger; Erin T Strovel; Miriam G Blitzer; Mark A Umbarger; Caleb Kennedy; Brian Bishop; Patrick Saunders; Gregory J Porreca; Jaclyn Schienda; Jocelyn Davie; Stephanie Hallam; Charles Towne
Journal:  Mol Genet Genomic Med       Date:  2013-09-16       Impact factor: 2.183

  7 in total

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