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PMID: 1897529 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi Jews.

American journal of human genetics ·Vol. 49 ·No. 4 ·1991-10-00 ·Pages 855-9

Zimran A, Gelbart T, Westwood B, Grabowski GA, Beutler E

Abstract

Reliable estimates of the frequency of Gaucher disease-producing mutations are not available. The high frequency of Gaucher disease in the Ashkenazi Jewish population is due to the occurrence of a mutation at nucleotide (nt) 1226. We have screened 593 DNA samples from normal Ashkenazi Jews, as well as 62 DNA samples from all our Ashkenazi Jewish patients with Gaucher disease, for the presence of the 1226 mutation. In the 593 presumed normal Ashkenazi Jewish individuals the 1226 mutation was identified in the heterozygous state in 37 and in the homozygous state in two, giving a gene frequency of .035 for the mutation. This 1226 mutation represented 73% of the 124 Gaucher disease alleles in Jewish Gaucher disease patients. Accordingly we estimate that the gene frequency for Gaucher disease among the Ashkenazi Jewish population is .047, which is equivalent to a carrier frequency of 8.9% and a birth incidence of 1:450.

MeSH Terms
Adolescent Adult Aged Gaucher Disease/epidemiology,genetics Gene Frequency Genetic Testing Heterozygote Humans Jews/genetics Middle Aged Mutation/genetics Tay-Sachs Disease/epidemiology,genetics
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Zimran A
Department of Medicine, Shaare Zedek Medical Center, Jerusalem.
Gelbart T
Westwood B
Grabowski G A
Beutler E
References (14)
14 references, click to expand
  1. Gaucher's disease without splenomegaly. Oldest patient on record, with review.
    N Y State J Med. 1962 Jul 15;62:2346-54 PMID: 13873139
  2. The facile detection of the nt 1226 mutation of glucocerebrosidase by 'mismatched' PCR.
    Clin Chim Acta. 1990 Dec 24;194(2-3):161-6 PMID: 2093469
  3. Gaucher disease: molecular heterogeneity and phenotype-genotype correlations.
    Am J Hum Genet. 1989 Aug;45(2):212-25 PMID: 2502917
  4. Prediction of severity of Gaucher's disease by identification of mutations at DNA level.
    Lancet. 1989 Aug 12;2(8659):349-52 PMID: 2569551
  5. Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individuals.
    Proc Natl Acad Sci U S A. 1988 Apr;85(7):2349-52 PMID: 3353383
  6. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.
    N Engl J Med. 1987 Oct 15;317(16):985-90 PMID: 3657865
  7. Designed diagnostic restriction fragment length polymorphisms for the detection of point mutations in ras oncogenes.
    Oncogene Res. 1989;4(3):235-41 PMID: 2567980
  8. Molecular cloning and nucleotide sequence of human glucocerebrosidase cDNA.
    Proc Natl Acad Sci U S A. 1985 Nov;82(21):7289-93 PMID: 3864160
  9. Misuse of marrow examination in the diagnosis of Gaucher disease.
    Blood. 1990 Aug 1;76(3):646-8 PMID: 2116196
  10. Detection of the 1226 (Jewish) mutation for Gaucher's disease by color PCR. A means for studying the gene frequency of the disorder.
    Am J Clin Pathol. 1990 Jun;93(6):788-91 PMID: 2346136
  11. Linkage of the PvuII polymorphism with the common Jewish mutation for Gaucher disease.
    Am J Hum Genet. 1990 May;46(5):902-5 PMID: 1971142
  12. Gaucher's disease: unexpected diagnosis in three patients over seventy years old.
    Nouv Rev Fr Hematol. 1984;26(3):201-3 PMID: 6739289
  13. Gaucher's disease in an asymptomatic 72-year-old.
    JAMA. 1977 Jun 6;237(23):2529 PMID: 576973
  14. The diagnosis of the adult type of Gaucher's disease and its carrier state by demonstration of deficiency of beta-glucosidase activity in peripheral blood leukocytes.
    J Lab Clin Med. 1970 Nov;76(5):747-55 PMID: 5477334
Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1991-10-00
Pages
855-9
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1683177
Subset
IM
Grants
NIDDK NIH HHS · DK36639 · United States
NIDDK NIH HHS · DK36729 · United States
NCRR NIH HHS · RR00833 · United States
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