Multicystic dysplastic kidney (MCDK) is a common nonhereditary cystic dysplasia that can be detected antenatally. This disorder commonly manifests in utero and presents unilaterally; however, this patient’s case demonstrates bilateral MCDKs. The use of sonography is essential in diagnosing this disorder both antenatally and following birth. Bilateral MCDKs present as large anechoic cysts overtaking renal parenchyma and halting all normal renal physiologic functions. This case study demonstrates the importance of early detection, the progression of this disorder, as well as the large part sonographic imaging plays in visualizing the MCDK.