Autosomaldominantpolycystickidneydisease(ADPKD) isacommonandcomplexhereditary nephropathy. Although most patients develop symptoms after adults, theybegin to bud in their fetal period. However, the un
Autosomal dominant polycystic kidney disease (ADPKD) is the most prevalent potentially lethal monogenic disorder. Mutations in the PKD1 gene, which encodes polycystin-1 (PC1), account for approximatel
Baseline demographics and clinical characteristics for female (n = 251) and male (n = 290) patients with ADPKD are reported separately, and for both sexes combined (n = 541). Data show mean ± standard
