Literature DB >> 12244559

Association of nonsyndromic Wilms tumor with premature centromere division (PCD).

K Méhes1, P Kajtár, G Kosztolányi.   

Abstract

Wilms tumor was discovered in a 22-month-old otherwise healthy girl. Her pretreatment karyotype proved to be normal 46,XX with total premature division (PCD) in 21% of her lymphocyte mitoses. This phenomenon was not seen in the parents. PCD was found in less than 4% of lymphocyte mitoses of five other children with Wilms tumor. The individual finding provides further evidence for a relation of PCD to tumorigenesis; however, elucidation of the question needs further systematic studies. Copyright 2002 Wiley-Liss, Inc.

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Mesh:

Year:  2002        PMID: 12244559     DOI: 10.1002/ajmg.10661

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


  3 in total

1.  Premature chromatid separation is not a useful diagnostic marker for Cornelia de Lange syndrome.

Authors:  Paola Castronovo; Cristina Gervasini; Anna Cereda; Maura Masciadri; Donatella Milani; Silvia Russo; Angelo Selicorni; Lidia Larizza
Journal:  Chromosome Res       Date:  2009-08-19       Impact factor: 5.239

2.  Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome.

Authors:  Maninder Kaur; Cheryl DeScipio; Jennifer McCallum; Dinah Yaeger; Marcella Devoto; Laird G Jackson; Nancy B Spinner; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2005-09-15       Impact factor: 2.802

Review 3.  Clinical manifestations of genetic instability overlap one another.

Authors:  Károly Méhes; György Kosztolányi
Journal:  Pathol Oncol Res       Date:  2004-03-18       Impact factor: 3.201

  3 in total

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