| Literature DB >> 31248877 |
Jorge Di Paola1, Christopher C Porter2.
Abstract
Germ line mutations in ETV6 are responsible for a familial thrombocytopenia and leukemia predisposition syndrome. Thrombocytopenia is almost completely penetrant and is usually mild. Leukemia is reported in ∼30% of carriers and is most often B-cell acute lymphoblastic leukemia. The mechanisms by which ETV6 dysfunction promotes thrombocytopenia and leukemia remain unclear. Care for individuals with ETV6-related thrombocytopenia and leukemia predisposition includes genetic counseling, treatment or prevention of excessive bleeding and surveillance for the development of hematologic malignancy.Entities:
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Year: 2019 PMID: 31248877 PMCID: PMC6706811 DOI: 10.1182/blood.2019852418
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113