Volume 34, Issue 4 pp. 601-605
Article
Full Access

Tay-Sachs disease carrier screening: Follow-up of a case-finding approach

Dr. J. T. R. Clarke M.D., Ph.D.

Corresponding Author

Dr. J. T. R. Clarke M.D., Ph.D.

Division of Clinical Genetics, Departments of Genetics and Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada

Division of Clinical Genetics, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, Canada M5G 1X8Search for more papers by this author
M. A. Skomorowski

M. A. Skomorowski

Division of Clinical Genetics, Departments of Genetics and Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada

Search for more papers by this author
S. Zuker

S. Zuker

Division of Clinical Genetics, Departments of Genetics and Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada

Search for more papers by this author
First published: December 1989
Citations: 8

Abstract

In order to determine the status of Tay-Sachs disease carrier identification in Toronto, Canada, since a change was made in 1978 from testing in the context of large-scale community clinics (up to 1,200 individuals tested in 1 day) to a case-finding approach to screening, a sample of area Jews was surveyed by questionnaire. The results indicated that a trend has developed for individuals at risk to delay testing until pregnancy when carrier detection is technically more difficult and the time available for retesting and organizing prenatal diagnosis is limited. If the trend continues, the full potential of chorionic villus sampling (CVS) for the prenatal diagnosis of the disease will be difficult to realize.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.