| Literature DB >> 33735874 |
Marisa J L Aitken1,2, Christopher B Benton1,3, Ghayas C Issa1, Koji Sasaki1, Musa Yilmaz1, Nicholas J Short4.
Abstract
CML is defined by the presence of an oncogenic fusion protein caused by a reciprocal translocation between chromosomes 9q and 22q. While our molecular understanding of CML pathogenesis has revolutionized drug development for this disease, we have yet to identify many predisposing factors for CML. Familial occurrence of CML has been rarely reported. Here, we describe 2 cases of CML in a 24-year-old woman and in her 73-year-old maternal great aunt. We describe genetic variants in these patients and report on their environmental exposures that may have contributed to CML pathogenesis. The possible familial association of these 2 cases of CML warrants further investigation into more definitive etiologies of this disease.Entities:
Keywords: Chronic myeloid leukemia; Familial cancer; Hereditary cancer syndromes
Mesh:
Year: 2021 PMID: 33735874 PMCID: PMC8448803 DOI: 10.1159/000513925
Source DB: PubMed Journal: Acta Haematol ISSN: 0001-5792 Impact factor: 2.195