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First report of t(1;9)(q21;q34) in Fanconi anemia as a preceeding chromosomal aberration before leukemia development

  • Istinye University

Research output: Contribution to journalArticlepeer-review

Abstract

Patients with Fanconi anemia (FA) tend to develop various hematologic and solid tumors. Cytogenetic abnormalities such as translocations of chromosome 1q, monosomy 5 and 7, trisomy 10, gains of 3q and t(8;21) have been reported in patients with FA who developed hematological malignancies. Since survival is low after the development of leukemia in FA patients, the follow-up for leukemia progression is very important. For this reason, cytogenetic anomalies that can be used as biomarkers in the development of leukemia are needed. Herein, we describe a patient with FA who developed acute myeloid leukemia with der(9)t(1;9) (q21;q34) for the first time.

Original languageEnglish
Pages (from-to)119-122
Number of pages4
JournalJournal of the Kuwait Medical Association
Volume54
Issue number1
Publication statusPublished - Mar 2022

Keywords

  • Fanconi anemia
  • acute myeloid leukemia
  • childhood leukemia
  • chromosomal abnormalities
  • rare translocation

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