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