본문으로 건너뛰기
← 뒤로

A Review of CEBPA's Role in Hereditary Leukemia.

EJHaem 2026 Vol.7(2) p. e70236

Rakiewicz T, Palmisiano N

📝 환자 설명용 한 줄

[BACKGROUND] Advances in genetic testing have allowed for extensive testing and identification of previously unrecognized inherited conditions; a prominent area of this research includes familial patt

이 논문을 인용하기

BibTeX ↓ RIS ↓
APA Rakiewicz T, Palmisiano N (2026). A Review of CEBPA's Role in Hereditary Leukemia.. EJHaem, 7(2), e70236. https://doi.org/10.1002/jha2.70236
MLA Rakiewicz T, et al.. "A Review of CEBPA's Role in Hereditary Leukemia.." EJHaem, vol. 7, no. 2, 2026, pp. e70236.
PMID 41769222
DOI 10.1002/jha2.70236

Abstract

[BACKGROUND] Advances in genetic testing have allowed for extensive testing and identification of previously unrecognized inherited conditions; a prominent area of this research includes familial patterns of acute myeloid leukemia (AML). Recognition of familial related hematologic malignancies can have lasting implications for both patients and their treatment plans, as well as their families.

[AIMS] This review summarizes the specific familial AML disease, CCAAT/enhancer binding protein-alpha (CEBPA) associated AML.

[CONTENT] We highlight CEBPA's function, pathogenesis, and potential treatment considerations after identification of the pathogenic or likely pathogenic (P/LP) germline mutations in cases of AML. Discussion of testing and screening for affected family members is also reviewed.

[SUMMARY] Identification of CEBPA familial AML is necessary for appropriate treatment planning and has additional implications for familial testing and screening. Clinical practice is still evolving treatment paradigms for these patients and their families. : The authors have confirmed clinical trial registration is not needed for this submission.