Male infertility: Pathogenesis and clinical diagnosis

被引:345
作者
Krausz, Csilla [1 ]
机构
[1] Dept Clin Physiopathol, Androl Unit, I-50137 Florence, Italy
关键词
male infertility; hypogonadism; genetics; cryptorchidism; Y chromosome; caryotype; spermatogenesis; assisted reproductive techniques (ART); HUMAN Y-CHROMOSOME; REVERSIBLE KALLMANN-SYNDROME; RECEPTOR GENE-MUTATIONS; PARTIAL AZFC DELETIONS; KLINEFELTER-SYNDROME; MEN; AZOOSPERMIA; POLYMORPHISMS; VARICOCELE; GR/GR;
D O I
10.1016/j.beem.2010.08.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Infertility affects about 7% of all men. The etiology of impaired sperm production and function can be related to factors acting at pre-testicular, post-testicular or directly at the testicular level. Primary testicular failure accounts for about 75% of all male factor infertility. Genetic factors can be identified in about 15% of cases (congenital hypogonadotrophic hypogonadism, congenital absence of vas deferens, primitive testicular failure). Despite progresses, mainly in the field of genetics, the etiology is still unknown in about 50% cases and it is termed "idiopathic infertility". A part from few exceptions, the only available therapy for male factor infertility is assisted reproduction which allows conception also in severe male factor, including azoospermia following testicular sperm extraction. The complete diagnostic workup is important for: i) the identification of treatable/reversible or health-threatening conditions; ii) selection of patients for assisted reproductive techniques; iii) for appropriate genetic counselling including preventive measures (preimplanatation or prenatal diagnosis) to safeguard the health of future offspring. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:271 / 285
页数:15
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