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A case of a novel PML/RARA short fusion transcript with truncated transcription variant 2 of the RARA gene.

Authors :
Jezísková I
Rázga F
Gazdová J
Doubek M
Jurcek T
Korístek Z
Mayer J
Dvoráková D
Source :
Molecular diagnosis & therapy [Mol Diagn Ther] 2010 Apr 01; Vol. 14 (2), pp. 113-7.
Publication Year :
2010

Abstract

Acute promyelocytic leukemia (APL) with atypical breakpoints in the promyelocytic leukemia (PML) and retinoic acid receptor-alpha (RARA) genes represents a rare leukemic event, which occurs preferentially in patients with variant types of the PML/RARA fusion gene. Here we report on a patient with APL with a unique PML/RARA fusion transcript that harbors a short type of this fusion gene, exhibiting unexpected results of standard PCR diagnostics. The detected transcript originates from fusion of PML exon 4 and a truncated form of transcription variant 2 of the RARA gene, with an additional 9 bp insertion. According to our knowledge, this differs from all previously described fusion transcripts.

Details

Language :
English
ISSN :
1179-2000
Volume :
14
Issue :
2
Database :
MEDLINE
Journal :
Molecular diagnosis & therapy
Publication Type :
Academic Journal
Accession number :
20359255
Full Text :
https://doi.org/10.2165/11317400-000000000-00000