Hemolytic Uremic Syndrome and Autosomal Dominant Interstitial Nephritis Report

Hemolytic Uremic Syndrome and Autosomal Dominant Interstitial Nephritis Reports

Hemolytic Uremic Syndrome and Autosomal Dominant Interstitial Nephritis are two medical conditions affecting the excretory system. The first has an infectious origin but there are atypical, rarer forms whose onset is genetic in nature. The second involves, however, a picture of progressive renal failure, tubulointerstitial nephropathy and bland urinary sediment, in absence of glomerular lesions. Its etiology is exclusively genetic.

40 genes analyzed

It is recommended if:

This panel is particularly suitable for those who experience signs and symptoms of atypical HUS, affecting the microvascular system of the kidneys, and for those who experience early polyuria, nocturia, salt craving, gout and weakness, which may represent the symptom of ADTKD.

List of main conditions:

• Glomerulosclerosis, focal segmental, 6
• Nephrotic syndrome, type 6
• Glomerulosclerosis, focal segmental, 2