Mutations in non-muscle myosin IIa (Myh9), lead to nephrotic syndrome in association with deafness, macrothrombocytopenia, and leukocyte inclusions in several syndromes such as Fechtner and Epstein syndromes, which might collectively be termed “Myh9 related diseases” [13]–[15]. Here, MYH9 is linked to macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss.