Cryptorchidism and Fertility
Author(s) -
Fatma Fawzy,
Amr H. Hussein,
Mostafa Mahmoud Eid,
Ahmed Mahmoud El Kashash,
Hosni Salem
Publication year - 2015
Publication title -
clinical medicine insights reproductive health
Language(s) - English
Resource type - Journals
ISSN - 1179-5581
DOI - 10.4137/cmrh.s25056
Subject(s) - maldevelopment , medicine , scrotum , infertility , fertility , gynecology , population , male infertility , orchiopexy , surgery , pregnancy , anatomy , biology , environmental health , genetics
Cryptorchidism, the failure of one or both testes to descend into the scrotum prenatally, occurs in 2.4%-5% of newborns. Many of these testes will descend spontaneously shortly after birth, but ~23% will remain undescended unless surgery is performed. Bilaterally cryptorchid men have a six times greater risk of being infertile when compared with unilaterally cryptorchid men and the general male population. Approximately 10% of infertile men have a history of cryptorchidism and orchidopexy. The main reasons for infertility in men with a history of cryptorchidism treated by orchidopexy are maldevelopment of the testes and an improper environment for the normal development of the testes, hyperthermia, and antisperm antibodies.
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