SCREENING FOR CARRIERS OF TAY-SACHS-DISEASE IN THE ULTRAORTHODOX ASHKENAZI JEWISH-COMMUNITY IN ISRAEL

被引:48
作者
BROIDE, E
ZEIGLER, M
ECKSTEIN, J
BACH, G
机构
[1] HADASSAH UNIV HOSP,DEPT HUMAN GENET,IL-91120 JERUSALEM,ISRAEL
[2] DOR YESHURIM ORG,NEW YORK,NY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 47卷 / 02期
关键词
HEX-A ACTIVITY; PRENATAL DIAGNOSIS; HETEROZYGOTES;
D O I
10.1002/ajmg.1320470214
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:213 / 215
页数:3
相关论文
共 9 条
[1]   SYNTHESIS OF 4-METHYLUMBELLIFERYL-BETA-D-N-ACETYLGLUCOSAMINE-6-SULFATE AND ITS USE IN CLASSIFICATION OF GM2 GANGLIOSIDOSIS GENOTYPES [J].
BAYLERAN, J ;
HECHTMAN, P ;
SARAY, W .
CLINICA CHIMICA ACTA, 1984, 143 (02) :73-89
[2]  
KABACK MM, 1981, LYSOSOMES LYSOSOMAL, P331
[3]  
KABACK MM, 1977, TAY SACHS DISEASE SC, P13
[4]  
KAMPINE JP, 1966, SCIENCE, V155, P85
[5]  
KRESSE H, 1981, J BIOL CHEM, V256, P2926
[6]   TAY-SACHS DISEASE - DETECTION OF HETEROZYGOTES AND HOMOZYGOTES BY SERUM HEXOSAMINIDASE ASSAY [J].
OBRIEN, JS ;
OKADA, S ;
CHEN, A ;
FILLERUP, DL .
NEW ENGLAND JOURNAL OF MEDICINE, 1970, 283 (01) :15-&
[7]  
PETERSEN GM, 1983, AM J HUM GENET, V35, P1258
[8]  
Sandhoff K., 1989, METABOLIC BASIS INHE, P1807
[9]  
VECHT J, 1983, ISRAEL J MED SCI, V19, P67