Chromosomal instability associated with adverse outcome: a case report of patient with Nijmegen breakage syndrome and rapidly developed T-NHL with complex karyotype

BACKGROUND: Nijmegen breakage syndrome (NBS) is a rare genetic disorder inherited in an autosomal recessive pattern associated with an increased risk of developing lymphoproliferative disorders, mainly non-Hodgkin lymphoma (NHL) and acute lymphoblastic leukemia (ALL). NBS patients are 50 times more...

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Detalles Bibliográficos
Autores principales: Włodarczyk, Monika, Lejman, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441545/
https://www.ncbi.nlm.nih.gov/pubmed/32843899
http://dx.doi.org/10.1186/s13039-020-00505-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441545/
https://www.ncbi.nlm.nih.gov/pubmed/32843899
http://dx.doi.org/10.1186/s13039-020-00505-2

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