Literature DB >> 3857858

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

E Seemanová, E Passarge, D Beneskova, J Houstĕk, P Kasal, M Sevcíková.   

Abstract

We describe nine patients with an apparently new genetic disorder characterized by: microcephaly with normal intelligence; "bird"-like facial appearance; cellular and humoral immune defects; and increased risk for lymphoreticular malignancies. The postmortem findings of five patients are described. Chromosome instability appears not to be a component of the disorder. The occurrence in three pairs of sibs and isonomy in another family suggests autosomal recessive inheritance.

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Year:  1985        PMID: 3857858     DOI: 10.1002/ajmg.1320200410

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  22 in total

1.  The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.

Authors:  K Saar; K H Chrzanowska; M Stumm; M Jung; G Nürnberg; T F Wienker; E Seemanová; R D Wegner; A Reis; K Sperling
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

2.  Noncomplementation of radiation-induced chromosome aberrations in ataxia-telangiectasia/ataxia-telangiectasia-variant heterodikaryons.

Authors:  M Stumm; K Sperling; R D Wegner
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

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

Review 4.  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

5.  Microcephaly and childhood non-Hodgkin's lymphoma.

Authors:  A Dluzniewska; D Tredowska-Skoczen; J Armata; J Tacik
Journal:  Arch Dis Child       Date:  1995-11       Impact factor: 3.791

6.  Increased bleomycin-induced chromosome damage in lymphocytes of patients with common variable immunodeficiency indicates an involvement of chromosomal instability in their cancer predisposition.

Authors:  I Vorechovsky; M Munzarova; J Lokaj
Journal:  Cancer Immunol Immunother       Date:  1989       Impact factor: 6.968

Review 7.  Nijmegen breakage syndrome. The International Nijmegen Breakage Syndrome Study Group.

Authors: 
Journal:  Arch Dis Child       Date:  2000-05       Impact factor: 3.791

8.  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

9.  Abnormalities in the T and NK lymphocyte phenotype in patients with Nijmegen breakage syndrome.

Authors:  J Michałkiewicz; C Barth; K Chrzanowska; H Gregorek; M Syczewska; C M B Weemaes; K Madaliński; J Stachowski
Journal:  Clin Exp Immunol       Date:  2003-12       Impact factor: 4.330

10.  Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma.

Authors:  Johanna M Schuetz; Amy C MaCarthur; Stephen Leach; Agnes S Lai; Richard P Gallagher; Joseph M Connors; Randy D Gascoyne; John J Spinelli; Angela R Brooks-Wilson
Journal:  BMC Med Genet       Date:  2009-11-16       Impact factor: 2.103

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