Literature DB >> 930922

Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim.

J German, D Bloom, E Passarge, K Fried, R M Goodman, I Katzenellenbogen, Z Laron, C Legum, S Levin.   

Abstract

An effort was made to identify all individuals with Bloom's syndrome living in Israel between September 1971 and September 1972. Each of the eight individuals located were Jewish and could readily be classified Ashkenazic. The frequency of the Bloom's syndrome gene in Ashkenazim was estimated to be .0042 (minimum), implying a heterozygote frequency greater than 1 in 120. A striking distortion of the sex ratio (M/F = 7.0) may have been due to underascertainment of affected females. One of the affected individuals ascertained during the survey subsequently has died from cancer, which is in keeping with the recognized cancer proneness of this condition. Four of the affected have married, but no conception is known to have occurred, which suggests that sub- or infertility is a feature of the syndrome.

Entities:  

Mesh:

Year:  1977        PMID: 930922      PMCID: PMC1685519     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  8 in total

1.  Founder effect in Tay-Sachs disease.

Authors:  A G Knudson
Journal:  Am J Hum Genet       Date:  1973-01       Impact factor: 11.025

2.  Founder effect in Tay-Sachs disease unlikely.

Authors:  N C Myrianthopoulos; A F Naylor; S M Aronson
Journal:  Am J Hum Genet       Date:  1972-05       Impact factor: 11.025

3.  Controversy in human genetics: founder effect in Tay-Sachs disease.

Authors:  G A Chase; V A McKusick
Journal:  Am J Hum Genet       Date:  1972-05       Impact factor: 11.025

4.  Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients.

Authors:  J German
Journal:  Am J Hum Genet       Date:  1969-03       Impact factor: 11.025

5.  The syndrome of congenital telangiectatic erythema and stunted growth.

Authors:  D Bloom
Journal:  J Pediatr       Date:  1966-01       Impact factor: 4.406

6.  Tay-Sachs disease: high gene frequency in a non-Jewish population.

Authors:  T E Kelly; G A Chase; M M Kaback; K Kumor; V A McKusick
Journal:  Am J Hum Genet       Date:  1975-05       Impact factor: 11.025

7.  A contribution to Bloom's syndrome. Congenital telangiectatic erythema resembling lypus erythematosus in dwarfs.

Authors:  I KATZENELLENBOGEN; Z LARON
Journal:  Arch Dermatol       Date:  1960-10

8.  Eye findings in congenital telangiectatic erythema and growth retardation (Bloom's syndrome).

Authors:  J Landau; I Katzenellenbogen; Z Laron
Journal:  Am J Ophthalmol       Date:  1966-10       Impact factor: 5.258

  8 in total
  15 in total

Review 1.  Human pyruvate kinase M2: a multifunctional protein.

Authors:  Vibhor Gupta; Rameshwar N K Bamezai
Journal:  Protein Sci       Date:  2010-11       Impact factor: 6.725

Review 2.  [Hereditary photodermatoses].

Authors:  P Poblete-Gutiérrez; W H C Burgdorf; C Has; M Berneburg; J Frank
Journal:  Hautarzt       Date:  2006-12       Impact factor: 0.751

Review 3.  Primary immunodeficiencies and their associated risk of malignancies in children: an overview.

Authors:  Samuele Renzi; Karin Petra Sabine Langenberg-Ververgaert; Nicolas Waespe; Salah Ali; Jack Bartram; Orli Michaeli; Julia Upton; Michaela Cada
Journal:  Eur J Pediatr       Date:  2020-03-11       Impact factor: 3.183

4.  Immunological lesions in human uracil DNA glycosylase: association with Bloom syndrome.

Authors:  G Seal; K Brech; S J Karp; B L Cool; M A Sirover
Journal:  Proc Natl Acad Sci U S A       Date:  1988-04       Impact factor: 11.205

Review 5.  Osteosarcoma: Molecular Pathogenesis and iPSC Modeling.

Authors:  Yu-Hsuan Lin; Brittany E Jewell; Julian Gingold; Linchao Lu; Ruiying Zhao; Lisa L Wang; Dung-Fang Lee
Journal:  Trends Mol Med       Date:  2017-07-20       Impact factor: 11.951

6.  Structural alterations of DNA ligase I in Bloom syndrome.

Authors:  A E Willis; R Weksberg; S Tomlinson; T Lindahl
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

7.  The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry.

Authors:  N A Ellis; S Ciocci; M Proytcheva; D Lennon; J Groden; J German
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

8.  BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome.

Authors:  Thiyam Ramsing Singh; Abdullah Mahmood Ali; Valeria Busygina; Steven Raynard; Qiang Fan; Chang-hu Du; Paul R Andreassen; Patrick Sung; Amom Ruhikanta Meetei
Journal:  Genes Dev       Date:  2008-10-15       Impact factor: 11.361

9.  [Genodermatoses with malignant skin tumors].

Authors:  L Hübinger; J Frank
Journal:  Hautarzt       Date:  2014-06       Impact factor: 0.751

10.  DNA ligase III is the major high molecular weight DNA joining activity in SV40-transformed human fibroblasts: normal levels of DNA ligase III activity in Bloom syndrome cells.

Authors:  A E Tomkinson; R Starr; R A Schultz
Journal:  Nucleic Acids Res       Date:  1993-11-25       Impact factor: 16.971

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