Log in to save to my catalogue

PAX5 alterations in an infant case of KMT2A‐rearranged leukemia with lineage switch

PAX5 alterations in an infant case of KMT2A‐rearranged leukemia with lineage switch

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9277256

PAX5 alterations in an infant case of KMT2A‐rearranged leukemia with lineage switch

About this item

Full title

PAX5 alterations in an infant case of KMT2A‐rearranged leukemia with lineage switch

Publisher

England: John Wiley & Sons, Inc

Journal title

Cancer science, 2022-07, Vol.113 (7), p.2472-2476

Language

English

Formats

Publication information

Publisher

England: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Lineage switch is a rare event at leukemic relapse. While mostly known to occur in KMT2A‐rearranged infant leukemia, the underlying mechanism is yet to be depicted. This case report describes a female infant who achieved remission of KMT2A‐MLLT3‐rearranged acute monocytic leukemia, but 6 months thereafter, relapsed as KMT2A‐MLLT3‐rearranged acute l...

Alternative Titles

Full title

PAX5 alterations in an infant case of KMT2A‐rearranged leukemia with lineage switch

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9277256

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9277256

Other Identifiers

ISSN

1347-9032

E-ISSN

1349-7006

DOI

10.1111/cas.15380

How to access this item