Genetics of Male Infertility

被引:45
作者
Hotaling, James M.
机构
[1] Division of Urology, Department of Surgery, School of Medicine, University of Utah, Salt Lake City, UT 84132
关键词
CONGENITAL BILATERAL ABSENCE; HUMAN Y-CHROMOSOME; INTRACYTOPLASMIC SPERM INJECTION; SINGLE-NUCLEOTIDE POLYMORPHISMS; POLYMERASE-CHAIN-REACTION; GENOME-WIDE ASSOCIATION; AZOOSPERMIA FACTOR AZF; PRDM9 MEISETZ GENE; KLINEFELTER-SYNDROME; CYSTIC-FIBROSIS;
D O I
10.1016/j.ucl.2013.08.009
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Genetics play an important role in the evaluation of the infertile male. The current limitations of classifying the genetic contribution to male infertility and the importance of phenotyping men are discussed, and the core concepts necessary to interpret most genetic studies are reviewed. The current genetic assays used clinically are discussed in detail. The use and interpretation of the cystic fibrosis transmembrane receptor assay are examined in the context of men with clinical bilateral absence of the vas deferens, a karyotype and Klinefelter syndrome, and Y chromosome microdeletions. The role of hormones and epigenetics in evaluating the genetic reproductive potential of men is discussed briefly. A summary of what the field might look like in 2034 is presented.
引用
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页码:1 / +
页数:18
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