Co-occurrence of PML-RARA gene fusion, chromosome 8 trisomy, and FLT3 ITD mutation in a young female patient with de novo acute myeloid leukemia and early death: A CARE case report

RATIONALE: Co-occurrence of cytogenetic and molecular abnormalities is frequently seen in patients with acute myeloid leukemia (AML). The clinical outcome and genetic abnormalities of AML may vary; therefore, genetic investigation must be complex, using several techniques, to have an appropriate cha...

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Detalles Bibliográficos
Autores principales: Tripon, Florin, Crauciuc, George Andrei, Bogliş, Alina, Moldovan, Valeriu, Sándor-Kéri, Johanna, Benedek, István Jr, Trifa, Adrian Pavel, Bănescu, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
4800
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220460/
https://www.ncbi.nlm.nih.gov/pubmed/32243411
http://dx.doi.org/10.1097/MD.0000000000019730

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220460/
https://www.ncbi.nlm.nih.gov/pubmed/32243411
http://dx.doi.org/10.1097/MD.0000000000019730

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