Acute promyelocytic leukemia with a cryptic insertion of RARA into PML on chromosome 15 due to uniparental isodisomy: A case report

Acute promyelocytic leukemia is a myeloid disorder that is characterized by the specific t(15;17) variant in ~98% of cases. The typical hypergranular and microgranular or hypogranular types exist, and are frequently associated with disseminated intravascular coagulopathy. Rare cases of promyelocytic...

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Detalles Bibliográficos
Autores principales: Venci, Anna, Mazza, Rita, Spinelli, Orietta, Di Schiena, Luciana, Bettio, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453168/
https://www.ncbi.nlm.nih.gov/pubmed/28599418
http://dx.doi.org/10.3892/ol.2017.5979

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453168/
https://www.ncbi.nlm.nih.gov/pubmed/28599418
http://dx.doi.org/10.3892/ol.2017.5979

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