Germline TP53 c.566C>T mutation incidentally diagnosed
during treatment for acute myeloid leukaemia: A case report
Abstract
A 53-year-old woman was admitted at our hospital for the treatment of
acute myeloid leukaemia. Heterozygous c.566C>T mutation in
the TP53 gene was found in leukaemia cells and germline cells. The
number of germline mutation found incidentally will increase. Therefore,
patients with such incidental findings must undergo adequate genetic
counselling.
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