• PMID: 18304229
• Gene Name: CFTR
• Condition: Congenital bilateral absence of vas deferens (CBAVD)
• Association: A CFTR gene mutation of I556V was found
• Mutation: I556V
• Population size: 1
• Population details: 1 Congenital bilateral absence of vas deferens (CBAVD)
• Age: 28 yrs
• Sex: Male
• Infertility type: Male infertility
• Other associated phenotypes: Congenital bilateral absence of vas deferens (CBAVD)

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation associated with a congenital bilateral absence of vas deferens

Sakamoto H, Yajima T, Suzuki K, Ogawa Y.

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations associated with cystic fibrosis have been reported to be rare in Japanese patients with congenital bilateral absence of vas deferens (CBAVD). A 28-year-old Japanese male was referred for infertility. Vas deferens and epididymis were not palpable bilaterally. Semen analyses showed azoospermia with volumes below 2.0 ml. Serum follicle-stimulating hormone value was slightly elevated. Seminal fructose concentration was also very low. Scrotal ultrasonography showed absence of the bodies and tails of the right and left epididymides. Imaging studies showed cystic dysplasia of the right seminal vesicle and agenesis of the left seminal vesicle. A CFTR gene mutation of I556V was found. Recent studies show that prevalence of CFTR gene mutation in Japanese CBAVD patients may be approximately equal to that of the Caucasian population. Genetic counselling may be recommended for any couple attempting assisted reproduction technology when the man has CBAVD. FAU - Sakamoto, Hideo AU - Sakamoto H AD - Department of Urology, Showa University School of Medicine, Tokyo, Japan. yuta_pitt@jcom.home.ne.jp FAU - Yajima, Takatoshi AU - Yajima T FAU - Suzuki, Kohta AU - Suzuki K