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PMID: 9781065 Published · ppublish English Journal Article

Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriers.

European journal of human genetics : EJHG ·Vol. 6 ·No. 2 ·1998-00-00 ·Pages 185-6

Peleg L, Frisch A, Goldman B, Karpaty M, Narinsky R, Bronstein S, Frydman M

Abstract

The heterozygote frequency of Gaucher disease (GD) and Tay-Sachs disease (TSD) is distinctly high among Ashkenazi Jews (1:29 for TSD and 1:16 for GD). Two main theories have been suggested to explain this high occurrence: a founder effect with subsequent genetic drift, and a selective advantage of heterozygotes. We compared the frequency of the GD most common mutation (1226A-->G) among carriers of the common TSD mutation (+1277 TATC) with the frequency of this mutation in the general Ashkenazi population. The frequency of GD carriers among 308 TSD heterozygotes was 1:28 which is about half the expected (P = 0.03). These results indicate that carriers of both diseases do not possess additional evolutionary advantage over single mutation carriers. A reasonable interpretation of these findings is that one or both mutations have arisen relatively recently in different regions of Europe and have not yet reached genetic equilibrium.

MeSH Terms
DNA Mutational Analysis Gaucher Disease/genetics Gene Frequency Heterozygote Humans Jews/genetics Tay-Sachs Disease/genetics
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Peleg L
Genetic Institute, Sheba Medical Center, Tel Hashomer, Israel.
Frisch A
Goldman B
Karpaty M
Narinsky R
Bronstein S
Frydman M
Article Info
Journal
European journal of human genetics : EJHG
Abbr.
Eur J Hum Genet
ISSN
1018-4813
Published
1998-00-00
Pages
185-6
Language
English
Region
England
NLM ID
9302235
Subset
IM
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