Literature DB >> 2491181

ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome.

C J Curry1, P O'Lague, J Tsai, H T Hutchison, N G Jaspers, D Wara, R A Gatti, H T Hutchinson.   

Abstract

This report describes twin girls with typical features of ataxia-telangiectasia, including increased alpha-fetoprotein, radio-resistant DNA synthesis, characteristic chromosome abnormality, and immunodeficiency. They have, in addition, microcephaly and mental retardation. Complementation studies were performed utilizing Sendai virus--mediated fusion of fibroblast cell lines. Complementation was observed with patients in ataxia-telangiectasia complementation groups A, C, and E but not with the cell line from a patient with the Nijmegen breakage syndrome, in which patients have microcephaly, radio-resistant DNA synthesis, chromosome aberrations, and immunodeficiency but lack ataxia and telangiectasia. These data suggest that the Nijmegen breakage syndrome and the patients described here are not genetically distinct entities but form a spectrum of one disorder.

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Year:  1989        PMID: 2491181      PMCID: PMC1683342     

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


  12 in total

1.  Variant of ataxia-telangiectasia with low-level radiosensitivity.

Authors:  M Fiorilli; A Antonelli; G Russo; M Crescenzi; M Carbonari; P Petrinelli
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  A chromosomal breakage syndrome with profound immunodeficiency.

Authors:  M E Conley; N B Spinner; B S Emanuel; P C Nowell; W W Nichols
Journal:  Blood       Date:  1986-05       Impact factor: 22.113

3.  Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia.

Authors:  N G Jaspers; R D Taalman; C Baan
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

4.  A new chromosome instability disorder.

Authors:  P Maraschio; D Peretti; S Lambiase; F Lo Curto; D Caufin; L Gargantini; L Minoli; O Zuffardi
Journal:  Clin Genet       Date:  1986-11       Impact factor: 4.438

5.  Genetic heterogeneity in ataxia-telangiectasia studied by cell fusion.

Authors:  N G Jaspers; D Bootsma
Journal:  Proc Natl Acad Sci U S A       Date:  1982-04       Impact factor: 11.205

6.  Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen Breakage Syndrome.

Authors:  R D Taalman; N G Jaspers; J M Scheres; J de Wit; T W Hustinx
Journal:  Mutat Res       Date:  1983-02       Impact factor: 2.433

7.  Autosomal recessive nonsyndromal microcephaly with normal intelligence.

Authors:  A S Teebi; S A Al-Awadi; A G White
Journal:  Am J Med Genet       Date:  1987-02

8.  Familial microcephaly with normal intelligence, immunodeficiency, and risk for lymphoreticular malignancies: a new autosomal recessive disorder.

Authors:  E Seemanová; E Passarge; D Beneskova; J Houstĕk; P Kasal; M Sevcíková
Journal:  Am J Med Genet       Date:  1985-04

9.  A new chromosomal instability disorder: the Nijmegen breakage syndrome.

Authors:  C M Weemaes; T W Hustinx; J M Scheres; P J van Munster; J A Bakkeren; R D Taalman
Journal:  Acta Paediatr Scand       Date:  1981-07

10.  Variant forms of ataxia telangiectasia.

Authors:  A M Taylor; E Flude; B Laher; M Stacey; E McKay; J Watt; S H Green; A E Harding
Journal:  J Med Genet       Date:  1987-11       Impact factor: 6.318

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  15 in total

Review 1.  The pathogenesis of ataxia-telangiectasia. Learning from a Rosetta Stone.

Authors:  R A Gatti; S Becker-Catania; H H Chun; X Sun; M Mitui; C H Lai; N Khanlou; M Babaei; R Cheng; C Clark; Y Huo; N C Udar; R K Iyer
Journal:  Clin Rev Allergy Immunol       Date:  2001-02       Impact factor: 8.667

2.  A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivity.

Authors:  R Tupler; G L Marseglia; M Stefanini; E Prosperi; L Chessa; T Nardo; A Marchi; P Maraschio
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

3.  Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region.

Authors:  O Sanal; S Wei; T Foroud; U Malhotra; P Concannon; P Charmley; W Salser; K Lange; R A Gatti
Journal:  Am J Hum Genet       Date:  1990-11       Impact factor: 11.025

4.  Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium.

Authors:  T Foroud; S Wei; Y Ziv; E Sobel; E Lange; A Chao; T Goradia; Y Huo; A Tolun; L Chessa; P Charmley; O Sanal; N Salman; C Julier; P Concannon; C McConville; A M Taylor; Y Shiloh; S K Lange; R A Gatti
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025

Review 5.  Nijmegen breakage syndrome.

Authors:  I van der Burgt; K H Chrzanowska; D Smeets; C Weemaes
Journal:  J Med Genet       Date:  1996-02       Impact factor: 6.318

6.  Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome.

Authors:  Y Ziv; M Frydman; E Lange; N Zelnik; G Rotman; C Julier; N G Jaspers; Y Dagan; D Abeliovicz; H Dar; Z Borochowitz; M Lathrop; R A Gatti; Y Shiloh
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

7.  Genotype-phenotype relationships in ataxia-telangiectasia and variants.

Authors:  S Gilad; L Chessa; R Khosravi; P Russell; Y Galanty; M Piane; R A Gatti; T J Jorgensen; Y Shiloh; A Bar-Shira
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

8.  Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations.

Authors:  M Telatar; S Teraoka; Z Wang; H H Chun; T Liang; S Castellvi-Bel; N Udar; A L Borresen-Dale; L Chessa; E Bernatowska-Matuszkiewicz; O Porras; M Watanabe; A Junker; P Concannon; R A Gatti
Journal:  Am J Hum Genet       Date:  1998-01       Impact factor: 11.025

9.  Human chromosome 11 complements ataxia-telangiectasia cells but does not complement the defect in AT-like Chinese hamster cell mutants.

Authors:  W Jongmans; J Wiegant; M Oshimura; M R James; P H Lohman; M Z Zdzienicka
Journal:  Hum Genet       Date:  1993-10-01       Impact factor: 4.132

10.  Severe microcephaly with normal intellectual development: the Nijmegen breakage syndrome.

Authors:  A J Green; J R Yates; A M Taylor; P Biggs; G M McGuire; C M McConville; C J Billing; N D Barnes
Journal:  Arch Dis Child       Date:  1995-11       Impact factor: 3.791

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