MYH9-RDs encompass an autosomal dominant inherited condition characterized by thrombocytopenia, giant platelets, and Döhle body-like inclusions.[4] These Döhle body-like inclusions can be observed in the cytoplasm of neutrophils, monocytes, eosinophils, and basophils in peripheral blood smears.[5] However, clinical misdiagnosis and oversight are common because of the tendency to overlook these inclusions, especially when they are faintly stained, and when laboratory personnel lack attentiveness and thoroughness, leading to missed diagnoses. This evidence concerns the gene MYH9 and Thrombocytopenia.