Literature DB >> 1153958

Isochromosome 17 in a case of eosinophilic leukaemia. An abnormality common to eosinophilic and neutrophilic cells.

F Mitelman, A Panani, L Brandt.   

Abstract

In a patient with eosinophilic leukaemia, serial chromosome studies using the Giemsa banding technique revealed a similar marker chromosome, identified as an isochromosome 17, in all bone marrow metaphases analysed. There was no Ph-1-chromosome. The cytogenetic data support the view that eosinophilic leukaemia is a specific disease entity, and suggest that both eosinophilic and neutrophilic cells are involved in the leukaemic process.

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Year:  1975        PMID: 1153958

Source DB:  PubMed          Journal:  Scand J Haematol        ISSN: 0036-553X


  3 in total

Review 1.  [Chromosome aberrations and the origin of tumors (author's transl)].

Authors:  H Zankl; K D Zang
Journal:  Klin Wochenschr       Date:  1978-01-01

2.  Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.

Authors:  L M Larson; W A Wasdahl; J H Saumur; M L Coleman; S M Jalal
Journal:  J Med Genet       Date:  1978-02       Impact factor: 6.318

3.  Eosinophilic leukaemia with trisomy 8 and double gammopathy.

Authors:  I Ribeiro; I R Carvalho; M Fontes; F Lima; R Matos; B A Anderson; L S Uva
Journal:  J Clin Pathol       Date:  1993-07       Impact factor: 3.411

  3 in total

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