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Home > Resources > A pediatric case of acute myeloid leukemia with KMT2A gene rearrangement t(10;11) and 16p11.2 microdeletion syndrome.
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A pediatric case of acute myeloid leukemia with KMT2A gene rearrangement t(10;11) and 16p11.2 microdeletion syndrome.

Proximal Deletion,

All,

This case report describes a child with 16p11.2 microdeletion syndrome who also developed acute myeloid leukemia (AML), a type of blood cancer, alongside a specific gene rearrangement (KMT2A), which may help families and doctors be aware of potential co-occurring medical conditions to watch for.

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Heme-Onc,

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