Literature DB >> 3802554

A new chromosome instability disorder.

P Maraschio, D Peretti, S Lambiase, F Lo Curto, D Caufin, L Gargantini, L Minoli, O Zuffardi.   

Abstract

Chromosome analysis in a 31-year-old woman referred for primary amenorrhea, revealed a very high incidence of chromosome aberrations. She had microcephaly and immunodeficiency. Her healthy parents were consanguineous (1/32) and a younger sister, also with primary amenorrhea, died when 20 years old with a malignant lymphoma. Chromosome studies were performed on lymphocytes and fibroblasts and in both tissues a high proportion of metaphases with multiple chromosome aberrations was found. Clonal and sporadic rearrangements, consisting of balanced and unbalanced translocations and dicentric chromosomes were more numerous than chromatid and chromosome breaks. In the lymphocytes the same unbalanced translocation t(8q;21q) was present in about 59% of the metaphases. Rearrangements involving chromosomes 7 and 14, similar to those described in patients with ataxia-telangiectasia were found, but with a lower frequency. Sister Chromatid Exchanges were not increased. Chromosome and chromatid abnormalities were enhanced after exposure of cells to mitomycin C but not after exposure to the radiomimetic drug bleomycin. Clinical and cytogenetic characteristics of the patient are compared with those of syndromes (Ataxia-Telangiectasia and Werner's syndrome) or isolated cases (Weemaes et al. 1981, Sperling 1983, Spinner et al. 1985) whose features are similar to those of our patient. This case might represent a new chromosome instability syndrome due to a recessive mutation.

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Year:  1986        PMID: 3802554     DOI: 10.1111/j.1399-0004.1986.tb01892.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  14 in total

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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
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Authors:  A Dluzniewska; D Tredowska-Skoczen; J Armata; J Tacik
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5.  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
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6.  Identification of variants in pleiotropic genes causing "isolated" premature ovarian insufficiency: implications for medical practice.

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7.  G2-phase radiation response in lymphoblastoid cell lines from Nijmegen breakage syndrome.

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8.  Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences.

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9.  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
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10.  ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome.

Authors:  C J Curry; P O'Lague; J Tsai; H T Hutchison; N G Jaspers; D Wara; R A Gatti; H T Hutchinson
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

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