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 journalArticlepeer-review

1 Scopus citations

Abstract

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
Volume25
Issue number3
StatePublished - 2008
Externally publishedYes

Keywords

  • All
  • Chromosome aberrations
  • Cytogenetics
  • Translocation

ASJC Scopus subject areas

  • Hematology

Fingerprint

Dive into the research topics of 'A childhood acute lymphoblastic leukemia (ALL) case with t(3;17)(q23;p13),t(5;12)(q31;p13),inv(11)(p15q12)'. Together they form a unique fingerprint.

Cite this