An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia

BACKGROUND: Myelodysplastic syndrome (MDS) is rare in the pediatric age group and it may be associated with inheritable bone marrow failure (BMF) such as Fanconi anemia (FA). FA is a rare multi-system genetic disorder, characterized by congenital malformations and progressive BMF. Patients with FA u...

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Bibliografiske detaljer
Udgivet i:Mol Cytogenet
Main Authors: Lovatel, Viviane Lamim, de Souza, Daiane Corrêa, Alvarenga, Tatiana Fonseca, Capela de Matos, Roberto R., Diniz, Claudia, Schramm, Marcia Trindade, Llerena Júnior, Juan Clinton, Silva, Maria Luiza Macedo, Abdelhay, Eliana, de Souza Fernandez, Teresa
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2018
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6042331/
https://ncbi.nlm.nih.gov/pubmed/30008805
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-018-0389-x
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