Novel WT1 and ACTN4 co-mutations in a patient with Denys-Drash syndrome and an atypical, potentially attenuated presentation of nephropathy: a case report.

backgroundDenys-Drash syndrome (DDS) is defined by early onset nephrotic syndrome rapidly progressing to end stage renal disease (ESRD) before 4 years of age, male pseudohermaphroditism, and Wilms tumor (WT). DDS is associated with mutations in the WT1 gene, most commonly in exons 8 or 9. ACTN4 mutations are associated with nephrotic syndrome and renal dysfunction, with an onset in early adulthood. CASE PRESENTATION: We present the case of an 18-year-old male with a past medical history of Wilms tumor (status post right nephrectomy, chemotherapy, and radiation during infancy), Denys-Drash syndrome, chronic kidney disease stage 2, and autism spectrum disorder. The patient presented to our clinic with worsening proteinuria discovered secondary to pyelonephritis. Genetic evaluation revealed a WT1 mutation, c.388_389insAC (p.Pro130Hisfs*34), complicated by an ACTN4 mutation, c.2698T > A (p.Ser900Thr). Under our care, his worsening proteinuria stabilized, and his estimated glomerular filtration rate (eGFR) remained at 83 mL/min/1.73 m2 (1.38 mL/s/1.73 m2), indicating preserved renal function. We used a multidisciplinary approach to manage this patient through lifestyle modification, regular monitoring, and conservative measures. Surveillance with regular ultrasounds and labs has been key in management. We chose to forgo biopsy because of the risk to the remaining kidney, and we will continue to evaluate the need for an angiotensin-converting enzyme (ACE) inhibitor on the basis of hemodynamic stability.

conclusionIn this case, we present a patient with delayed nephropathy in the presence of novel WT1 and ACTN4 mutations, suggesting the potential for a new genotype‒phenotype relationship of DDS or the attenuation of disease behavior. When diagnostic testing is limited due to increased risk to the patient, we emphasize the need for personalized treatment plans and a multimodal approach with close monitoring in the long-term management of such complicated cases. This case documents novel mutations, highlights the importance of genetic testing, and justifies further investigation into the relationship between genotype and phenotype for patients with mutations contributing to renal pathology. CLINICAL

trial registrationNot applicable.