Set-up of a Platform for Personalized Diagnosis of Rare Kidney Diseases (NIKE)

Inclusion Criteria

• •family history of kidney disease and/or parental consanguinity;
• •extra-renal involvement (e.g., sensorineural hearing loss);
• •resistance to treatment (e.g., immunosuppressive);
• •metabolic acidosis or metabolic alkalosis in the absence of renal failure;
• •ultrasound detection of of at least 2 cystic lesions in each kidney or nephrocalcinosis;
• •ultrasound detection of congenital abnormalities of the kidney and urinary tract (CAKUT) and CKD stage ≥ 2 according to KDIGO definition
• •informed consent form.