Molecular Pathology of Cryptorchidism-Induced Infertility
Author(s) -
María José Docampo,
Faruk Hadžiselimović
Publication year - 2015
Publication title -
sexual development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 44
eISSN - 1661-5433
pISSN - 1661-5425
DOI - 10.1159/000442059
Subject(s) - infertility , azoospermia , biology , gonad , gonadal dysgenesis , male infertility , disorders of sex development , sterility , andrology , endocrinology , medicine , genetics , pregnancy
Cryptorchidism is the most common cause of non-obstructive azoospermia in man. In contrast to the general belief that temperature-dependent effects on the undescended gonad damage cryptorchid testes before sexual maturation is complete, molecular pathology strongly supports the theory that impaired mini-puberty is responsible for azoospermia and infertility in cryptorchidism. Molecular biological observations favor LH deficiency, with EGR4 as a master regulatory gene in Leydig cell dysgenesis, as the reason for impaired mini-puberty, and recent evidence supports the idea that infertility in cryptorchidism is a consequence of alterations in the Piwi pathway.
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