Renal cysts and diabetes syndrome

Renal cysts and diabetes syndrome (RCAD) is a rare form of maturity-onset diabetes of the young (MODY) characterized clinically by heterogeneous cystic renal disease and early-onset familial non-autoimmune diabetes. Pancreatic atrophy, liver dysfunction and genital tract anomalies are also features of the syndrome.

Also known as: CAKUT with diabetes, HNF1B-MODY, HNF1B-related renal cysts and diabetes syndrome, MODY5, RCAD, RCAD syndrome, congenital anomalies of the kidney and urinary tract with diabetes, hepatocyte nuclear Factor 1-beta-associated monogenic diabetes

35 clinical trials for this condition and its sub-types, 0 tagged with Renal cysts and diabetes syndrome itself.