familial platelet disorder with associated myeloid malignancy
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Pathology
- qualitative & quantitative platelet defects
- propensity to develop acute myelogenous leukemia
Genetics
- autosomal dominant
- associated with defects in RUNX1
Laboratory
- CBC may show thrombocytopenia
- platelet aggregation may be abnormal
Complications
- propensity to develop acute myelogenous leukemia