Objective To evaluate the incidence of renal and seminal mutations (eight of 13 vs three of 10). Semen variables (pH<7.2, fructose <1 g/L and ejaculate volume vesicle (SV) abnormalities, and the presence or absence of CFTR gene mutations, in a cohort of patients <2 mL) did not diCerentiate patients with or without anomalies of the kidney, SV or with mutations, except referred for congenital bilateral absence of the vas deferens (CBAVD).in patients with a pH<7.2 for which renal anomalies were less frequent (two of 25 vs six of 16, P<0.05) Patients and method Forty-one patients with CBAVD, confirmed by surgical exploration, were evaluated by and mutations more frequent (19 of 25 vs five of 12, P<0.01). ultrasonography for renal and SV anomalies. Semen variables (pH, fructose level and ejaculate volume),Conclusion Renal anomalies associated with CBAVD should be considered as supporting maldevelopment sweat chloride levels and mutations of the 3, 4, 7, 9, 10, 11, 13, 14b, 17b, 19, 20 and 21 exons of the as a cause, but analysis of CFTR mutations in these cases should not be omitted. Unlike anomalies of the CFTR gene were determined. Result In eight patients with renal anomalies there were SV, a low ejaculate volume or low fructose level, a semen pH of <7.2 is the only nonspecific variable in no detectable mutations of CFTR, compared with 23 in the 33 patients with no renal anomalies (P<0.02).patients with CFTR mutations. Keywords Cystic fibrosis, azoospermia, kidney, seminal SV anomalies were not related to the presence or absence of mutations (11 of 23 vs 11 of 18), or in vesicle, malformations compound heterozygote patients carrying two (CFTR) responsible for cystic fibrosis were discovered,