Acute myeloid leukemia in a child with familial platelet disorder and a cryptic runx1 intragenic deletion

Lois M Dodson; Kristen J Kurtz; Andrea N Marcogliese; Brian D Friend; Alexandra M Stevens; Kevin E Fisher

doi:10.1080/08880018.2022.2035028

Acute myeloid leukemia in a child with familial platelet disorder and a cryptic runx1 intragenic deletion

Pediatr Hematol Oncol. 2022 Sep;39(6):580-585. doi: 10.1080/08880018.2022.2035028. Epub 2022 Feb 9.

Authors

Lois M Dodson¹, Kristen J Kurtz^{1

2

3}, Andrea N Marcogliese^{1

2

4}, Brian D Friend^{1

2

3

5}, Alexandra M Stevens^{1

2

3}, Kevin E Fisher^{1

2

4}

Affiliations

¹ Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
² Texas Children's Hospital, Houston, Texas, USA.
³ Section of Hematology/Oncology, Texas Children's Hospital, Houston, Texas, USA.
⁴ Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas, USA.
⁵ Center for Cell and Gene Therapy, Houston, Texas, USA.

PMID: 35135432
DOI: 10.1080/08880018.2022.2035028

No abstract available

Publication types

Letter

MeSH terms

Blood Platelet Disorders* / genetics
Child
Core Binding Factor Alpha 2 Subunit / genetics
Humans
Leukemia, Myeloid, Acute* / genetics
Mutation

Substances

Core Binding Factor Alpha 2 Subunit
RUNX1 protein, human