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
Link To Document :
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