Abstract
Subfertility in men is a heterogeneous syndrome, its pathophysiology remaining unknown in the majority of affected men. A large number of genes and loci are associated with sterility in experimental animals, but the human homologues of most of these genes have not been characterized. A British study suggested that, in a large proportion of men with idiopathic infertility, the disorder is inherited as an autosomal recessive trait; this provocative hypothesis needs confirmation. Because normal germ cell development requires the temporally and spatially co-ordinated expression of a number of gene products at the hypothalamic, pituitary and testicular levels, it is safe to predict that a large number of autosomal, as well as X- and Y-linked, genes will probably be implicated in different subsets of male subfertility.
| Original language | English |
|---|---|
| Pages (from-to) | 363-388 |
| Number of pages | 26 |
| Journal | Baillière's best practice |
| Volume | 14(3) |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 2000 |
ASJC Scopus subject areas
- Endocrinology
- Endocrinology, Diabetes and Metabolism