Literature DB >> 293233

Fanconi's anemia: terminal leukemia and "Forme fruste" in one family.

T M Schroeder, E Pöhler, H D Hufnagl, C Stahl-Maugé.   

Abstract

Two adult sisters are described. One with a full clinical, hematological and cytogenetic picture of Fanconi's anemia died of monocytic leukemia. The other woman has several malformations and clinical signs which are found in Fanconi's anemia, but does not show any hematological disorder or sign of bone marrow insufficiency. Cytogenetic findings in this case are comparable to those typical cases with Fanconi's anemia. This case is therefore considered to represent a "forme fruste" of Fanconi's anemia.

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Year:  1979        PMID: 293233     DOI: 10.1111/j.1399-0004.1979.tb00998.x

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


  2 in total

1.  Clinical and cytogenetic diversity in Fanconi's anaemia.

Authors:  G Duckworth-Rysiecki; M Hultén; J Mann; A M Taylor
Journal:  J Med Genet       Date:  1984-06       Impact factor: 6.318

2.  Chromosomal studies of leukemic and preleukemic Fanconii's anemia patients: examples of acquired 'chromosomal amplification.'.

Authors:  R Berger; A Bernheim; M Le Coniat; D Vecchione; G Schaison
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  2 in total

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