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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2018
Assuntos:
Case Report
Acesso em linha: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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