Article
[The detection of CFTR gene mutation in patients with azoospermia].
Ginekologia polska - 1 Jun 1998
Semczuk M, Kostuch M, Krzyzanowski A, Kwaśniewska A, Wojcierowski J
Abstract excerpt
Cystic fibrosis (CF) is the most common autosomal recessive disorder in Caucasian population that involves the lungs, pancreas, sweat glands, intestine, liver and reproductive tract. The majority of men with CF are infertile due to a bilateral congenital absence of the vas deferens (CBAVD). The p...
Topics
- Adult
- Chromosome Aberrations
- Chromosome Disorders
- Cystic Fibrosis Transmembrane Conductance Regulator
- Follicle Stimulating Hormone
- Genotype
- Humans
- Luteinizing Hormone
- Male
- Oligospermia
- Point Mutation
- Prolactin
- Testosterone
- Vas Deferens
