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- W4311456687 abstract "The genetic causes of male infertility are highly heterogeneous, and a large portion of these causes remains unexplained. More than 2300 testes-specific genes may contribute to male infertility [1]. Primary testicular disorders affecting spermatogenesis are commonly associated with abnormal semen parameters, including sperm concentration (oligozoospermia or azoospermia), morphology, motility, and vitality. Studies in infertile men have demonstrated that up to 20% carry constitutional chromosome aberrations [2–5]. Genomic aberrations found in these patients include numerical abnormalities, such as Klinefelter syndrome and its variants; XYY karyotype; testicular disorders of sex development, such as XX males; structural chromosome rearrangements, including Robertsonian translocations, balanced reciprocal translocations and inversions; as well as submicroscopic DNA copy number alterations (microdeletions and microduplications) encompassing genes associated with spermatogenesis or gonadal development." @default.
- W4311456687 created "2022-12-26" @default.
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- W4311456687 date "2023-01-05" @default.
- W4311456687 modified "2023-09-30" @default.
- W4311456687 title "Chromosomal Causes of Infertility" @default.
- W4311456687 doi "https://doi.org/10.1017/9781009197700.007" @default.
- W4311456687 hasPublicationYear "2023" @default.
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