Glomerular diseases are a large and heterogeneous group of pathologies. Clinically they can manifest with subtle symptoms, such as mild hematuria or proteinuria, to severe cases of nephritic syndrome, nephrotic syndrome, and/or kidney failure. Family history, refractoriness to immunosuppressive treatments, and manifestation at an early age, among others, are usually suggestive data. In this panel, the most clinically relevant genes in its development have been included.
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