In a case series by Oh et al., nephropathy was detected in 30% of MYH9-related disorder cases, with characteristic features definitive of early-onset proteinuria and rapidly progressing renal disease, similar to our own patient cases.11 Furthermore, another study by Pecci et al. also reported that 61 of 247 patients (roughly 25%) developed proteinuria and nephropathy.12 All of these studies, including our case series, incite further evaluation for the epidemiological bassline of MHA and associated nephropathy. This evidence concerns the gene MYH9 and Nephropathy.