Title of article
The genetic basis of infertility in men
Author/Authors
Shalender Bhasin، نويسنده , , Con Mallidis، نويسنده , , Kun Ma، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2000
Pages
26
From page
363
To page
388
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.
Keywords
genetics , Male Infertility , Y-chromosome deletions , autosomal loci for infertility , CFTR mutations , CREM mutations , intracytoplasmic sperm injection.
Journal title
Best Practice and Research Clinical Endocrinology and Metabolism
Serial Year
2000
Journal title
Best Practice and Research Clinical Endocrinology and Metabolism
Record number
465787
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