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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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2026-06-01
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| Serie: | Pediatric Hematology Oncology Journal |
| Soggetti: | |
| Accesso online: | http://www.sciencedirect.com/science/article/pii/S2468124526000276 |
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