Augarten A, Yahav Y, Kerem B S, Halle D, Laufer J, Szeinberg A, Dor J, Mashiach S, Gazit E, Madgar I
Department of Paediatrics, Chaim Sheba Medical Centre, Tel Hashomer, Israel.
Lancet. 1994 Nov 26;344(8935):1473-4. doi: 10.1016/s0140-6736(94)90292-5.
The high frequency of mutations in the cystic fibrosis gene in patients with congenital bilateral absence of vas deferens (CBAVD) has raised the question whether all of them have a genital form of cystic fibrosis. We investigated 47 CBAVD patients by ultrasonography, 10 (21%) had renal malformations and 37 (79%) did not. In the former group, no cystic fibrosis mutations were found and sweat chloride concentrations were normal. In the latter group, 18 patients (49%) carried at least one cystic fibrosis mutation and sweat chloride was high in 17 of 26 tested (65%). Our findings suggest that CBAVD patients with renal malformations do not necessarily have cystic fibrosis.