Literature DB >> 8182723

Acute myeloid leukaemia in a patient with Seckel syndrome.

A Hayani1, C R Suarez, Z Molnar, M LeBeau, J Godwin.   

Abstract

We report a female patient with Seckel syndrome who developed acute myeloid leukaemia at the age of 26 years. Analysis of bone marrow chromosomes showed an abnormal clone with abnormalities involving multiple chromosomes, including monosomy 7, trisomy 8, trisomy 11, and loss of the long arm of chromosome 5. After treatment with chemotherapy, the patient experienced severe toxicity with profound bone marrow aplasia and died of pneumonia two months later. We suggest that patients with Seckel syndrome may be at risk of developing myelodysplasia and acute myeloid leukaemia. They may also have poor tolerance to cytotoxic therapy.

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Year:  1994        PMID: 8182723      PMCID: PMC1049679          DOI: 10.1136/jmg.31.2.148

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  6 in total

1.  Familial dwarfism associated with microcephaly, mental retardation and anaemia.

Authors:  C UPJOHN
Journal:  Proc R Soc Med       Date:  1955-05

2.  Seckel's dwarfism: analysis of chromosome breakage and sister chromatid exchanges.

Authors:  J Cervenka; H Tsuchiya; T Ishiki; M Suzuki; H Mori
Journal:  Am J Dis Child       Date:  1979-05

3.  Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?

Authors:  M G Butler; B D Hall; R N Maclean; C B Lozzio
Journal:  Am J Med Genet       Date:  1987-07

Review 4.  Bone marrow transplantation for Fanconi anemia.

Authors:  E Gluckman; R Berger; J Dutreix
Journal:  Semin Hematol       Date:  1984-01       Impact factor: 3.851

5.  Constitutional hypoplastic anemia associated with familial "bird-headed" dwarfism (Seckel syndrome).

Authors:  J S Lilleyman
Journal:  Am J Pediatr Hematol Oncol       Date:  1984

Review 6.  Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome.

Authors:  F Majewski; T Goecke
Journal:  Am J Med Genet       Date:  1982-05
  6 in total
  12 in total

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2.  Severe intrauterine growth retardation with increased mitomycin C sensitivity: a further chromosome breakage syndrome.

Authors:  C G Woods; M Leversha; J G Rogers
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9.  Fecalith causing intestinal obstruction in a patient with seckel syndrome.

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