Screening for carriers of Tay-Sachs disease in the ultraorthodox Ashkenazi Jewish community in Israel

E. Broide, M. Zeigler, J. Eckstein, G. Bach

Research output: Contribution to journalArticlepeer-review


A screening program for the detection of Tay-Sachs disease (TSD) carriers in the ultra Orthodox community of Ashkenazi Jews has operated in Israel since 1986. The purpose of this program is the prevention of marriages of 2 heterozygotes. The screened individuals are mostly couples in the engagement process or students in religious high schools. Two mandatory requirements guide this program. First, anonymity of the tested individuals who are identified only by code numbers; second completion of the test results of couples in the engagement process within a few days. The screening program is performed by the determination of hexosaminidase A (Hex A) activity in serum which is repeated in serum and leukocyte extracts in couples where both partners were found in the heterozygote range in the initial tests. The minimal carrier frequency was estimated to be 1:26 or higher, which is higher then in the general Jewish Ashkenazi population. This higher carrier frequency apparently stems from the fact that most members of this community originate from central Europe where the TSD carrier frequency was previously reported to be the highest in the Ashkenazi population. Since the beginning of the screening program no TSD child has been born to newlywed couples of this community in Israel.

Original languageEnglish
Pages (from-to)213-215
Number of pages3
JournalAmerican Journal of Medical Genetics
Issue number2
StatePublished - 1993
Externally publishedYes


  • Hex A activity
  • heterozygotes
  • prenatal diagnosis


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