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Familial acute myeloid leukemia with germline CEBPA mutation in a Syrian family: successfully treated with allogeneic hematopoietic stem cell transplantation

Background: Familial acute myeloid leukemia (AML) associated with germline CEBPA mutations is a rare autosomal dominant disorder. Early recognition and genetic testing are essential for diagnosis, management, and donor selection in affected families. Case presentation: We report a Syrian family with...

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Principais autores: Hind Alhiraki, Maged Kheder
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2026-06-01
Serier:Pediatric Hematology Oncology Journal
Fag:
Familial AML
CEBPA mutation
Allogeneic HSCT
Pediatric leukemia
Complete remission
Online adgang:http://www.sciencedirect.com/science/article/pii/S2468124526000276
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