A childhood acute lymphoblastic leukemia (ALL) case with t(3;17)(q23;p13),t(5;12)(q31;p13),inv(11)(p15q12)

Ayşe Çirakoǧlu, Yelda Tarkan-Argüden, Ayhan Devireń, Dilhan Kuru, Şükriye Yilmaz, Su Gülsün Berrak, Cengiz Canpolat, Seniha Hacihanefioǧlu

Research output: Contribution to journalArticle


It is known that clonal chromosomal changes in childhood ALL are nonrandom and important markers for diagnosis, prognosis and relaps. In this report we present 4 year-old boy with ALL-L1 who has complex chromosomal rearrangements. Chromosome analysis was performed on bone marrow aspiration sample in relaps after one year from diagnosis and induction chemotherapy. The karyotype was; 46,XY,t(3;17)(q23;p13),t(5;12)(q31;p13),inv(11)(p15q12) [11]/46,XY[8] (Turk J Hematol 2006, 25: 152-4).

Original languageEnglish (US)
Pages (from-to)152-154
Number of pages3
JournalTurkish Journal of Hematology
Issue number3
StatePublished - Oct 10 2008


  • All
  • Chromosome aberrations
  • Cytogenetics
  • Translocation

ASJC Scopus subject areas

  • Hematology

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    Çirakoǧlu, A., Tarkan-Argüden, Y., Devireń, A., Kuru, D., Yilmaz, Ş., Berrak, S. G., Canpolat, C., & Hacihanefioǧlu, S. (2008). A childhood acute lymphoblastic leukemia (ALL) case with t(3;17)(q23;p13),t(5;12)(q31;p13),inv(11)(p15q12). Turkish Journal of Hematology, 25(3), 152-154.