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
Autosomaldominantpolycystickidneydisease(ADPKD) isacommonandcomplexhereditary nephropathy. Although most patients develop symptoms after adults, theybegin to bud in their fetal period. However, the un
