Literature DB >> 11996797

New cytogenetic variant, insertion (15;17)(q22;q12q21), in an adolescent with acute promyelocytic leukemia.

Raj Rolston1, Karen E Weck, Jean M Tersak, Maureen E Sherer, Kathleen Cumbie, Sofia Shekhter-Levin.   

Abstract

We present the case of a 15-year-old female with acute promyelocytic leukemia and a new variant chromosome rearrangement identified as ins(15;17)(q22;q12q21) by conventional cytogenetic analysis. This finding was confirmed by fluorescence in situ hybridization using the PML-RARA DNA probe and whole chromosome paints 15 and 17. A typical PML-RARA fusion transcript consistent with a breakpoint in intron 3 of the PML gene and intron 2 of the RARA gene was identified by reverse transcription polymerase chain reaction.

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Year:  2002        PMID: 11996797     DOI: 10.1016/s0165-4608(01)00595-7

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  1 in total

1.  Characterization of cryptic rearrangements, deletion, complex variants of PML, RARA in acute promyelocytic leukemia.

Authors:  Pratibha Kadam Amare; Chanda Baisane; Reena Nair; Hari Menon; Shripad Banavali; Sharayu Kabre; Sumit Gujral; P Subramaniam
Journal:  Indian J Hum Genet       Date:  2011-05
  1 in total

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