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Epidemiology of Genetic Disorders in Male Infertility

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Abstract

Infertility has become a major social concern, with high demand for treatment. Due to the high prevalence of genetic abnormalities among men suffering from infertility with severe oligozoospermia and azoospermia, cytogenetic testing is highly warranted. These tests can diagnose some, but not all, of the causes of poor reproductive potential in men. Unfortunately, these genetic tests are considered a monetary burden to some patients. As a result, these patients are deprived of the proper diagnosis and treatment for their infertility problems. In addition, these genetic tests are not readily available in centres, especially in developing countries, and are not covered by insurance. Genetic diagnoses are valuable for the determination of the prognosis, decisions regarding treatment options and management for both the male partner and the couple as a whole. Inadequate evaluation of the genetic causes of male infertility may affect management due to a lack of proper counselling and the suboptimal prevention of vertical transmission of genetic defects during assisted reproductive technologies. Despite recent advances in technology and diagnostic examinations, many men do not have identifiable causes of their infertility. The epidemiology of male infertility is difficult to study for several reasons. There are considerable variations in the frequency of male infertility and its aetiologies worldwide, and its nature has been poorly studied in heterogeneous data. Knowing the global epidemiology of different causes of infertility is fundamental for the effective delivery of care to these affected individuals. Only a handful of large-scale studies have addressed the epidemiology of genetic aetiologies of male infertility, and the published data are littered with significant shortcomings. Further high-quality methodological studies are needed to establish the true epidemiology of each genetic cause of male infertility. A deep understanding of all the aspects of the genetic conditions causing male infertility is needed in order to offer infertile couples the most appropriate treatment for their disorders.

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References

  1. Zegers-Hochschild F, Adamson D, Dyer S, Racowsky C, de Mouzon J, Sokol R, et al. The International Glossary on infertility and fertility care. Fertil Steril. 2017;108(3):393–406.

    Article  PubMed  Google Scholar 

  2. Sharlip ID, Jarow JP, Belker AM, Lipshultz LI, Sigman M, Thomas AJ, et al. Best practice policies for male infertility. Fertil Steril. 2002;77:873–82.

    Article  PubMed  Google Scholar 

  3. Thonneau P, Marchand S, Tallec A, Ferial ML, Ducot B, al e. Incidence and main causes of infertility in a resident population (1,850,000) of three French regions (1988-1989). Hum Reprod. 1991;6(6):811–6.

    Article  CAS  PubMed  Google Scholar 

  4. Olsen J, Küppers-Chinnow M, Spinelli A. Seeking medical help for subfecundity: a study based upon surveys in five European countries. Fertil Steril. 1996;66(1):95–100.

    Article  CAS  PubMed  Google Scholar 

  5. Bracke A, Peeters K, Punjabi U, Hoogewijs D, Dewilde S. A search for molecular mechanisms underlying male idiopathic infertility. Reprod Biomed Online. 2018;36(3):327–39. https://doi.org/10.1016/j.rbmo.2017.12.005. Epub 2017 Dec 27.

    Article  CAS  PubMed  Google Scholar 

  6. Krausz C. Male infertility: pathogenesis and clinical diagnosis. Best Pract Res Clin Endocrinol Metab. 2011;25(2):271–85. https://doi.org/10.1016/j.beem.2010.08.006.

    Article  PubMed  Google Scholar 

  7. Dohle GR, Halley DJ, Van Hemel JO, van den Ouwel AM, Pieters MH, et al. Genetic risk factors in infertile men with severe oligozoospermia and azoospermia. Hum Reprod. 2002;17(1):13–6.

    Article  CAS  PubMed  Google Scholar 

  8. Georgiou I, Syrrou M, Pardalidis N, Karakitsios K, Mantzavinos T, et al. Genetic and epigenetic risks of intracytoplasmic sperm injection method. Asian J Androl. 2006;8(6):643–73.

    Article  PubMed  Google Scholar 

  9. Povey AC, Stocks SJ. Epidemiology and trends in male subfertility. Hum Fertil (Camb). 2010;13(4):182–8. https://doi.org/10.3109/14647273.2010.515700.

    Article  CAS  Google Scholar 

  10. Boivin J, Bunting L, Collins JA, Nygren KG. International estimates of infertility prevalence and treatment-seeking: potential need and demand for infertility medical care. Hum Reprod. 2007;22(6):1506–12. Epub 2007 Mar 21.

    Article  PubMed  Google Scholar 

  11. Mascarenhas MN, Flaxman SR, Boerma T, Vanderpoel S, Stevens GA. regional, and global trends in infertility prevalence since 1990: a systematic analysis of 277 health surveys. PLoS Med. 2012;9(12):e1001356. https://doi.org/10.1371/journal.pmed.1001356. Epub 2012 Dec 18.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Eisenberg ML, Lathi RB, Baker VL, Westphal LM, Milki AA, Nangia AK. Frequency of the male infertility evaluation: data from the national survey of family growth. J Urol. 2013;189(3):1030–4. https://doi.org/10.1016/j.juro.2012.08.239. Epub 2012 Sep 23.

    Article  PubMed  Google Scholar 

  13. Agarwal A, Mulgund A, Hamada A, Chyatte MR. Unique view on male infertility around the globe. Reprod Biol Endocrinol. 2015;13:37. https://doi.org/10.1186/s12958-015-0032-1.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Ikechebelu JI, Adinma JI, Orie EF, Ikegwuonu SO. High prevalence of male infertility in southeastern Nigeria. J Obstet Gynaecol. 2003;23(6):657–9.

    Article  CAS  PubMed  Google Scholar 

  15. Philippov OS, Radionchenko AA, Bolotova VP, Voronovskaya NI, Potemkina TV. Estimation of the prevalence and causes of infertility in western Siberia. Bull World Health Organ. 1998;76(2):183–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  16. Aflatoonian A, Seyedhassani SM, Tabibneijad N. The epidemiological and etiological aspects of infertility in Yazd province of Iran. Iran J Reprod Med. 2009;7(3):117–22.

    Google Scholar 

  17. Bablok L, Dziadecki W, Szymusik I, Wolczynski S, Kurzawa R, et al. Patterns of infertility in Poland - multicenter study. Neuro Endocrinol Lett. 2011;32(6):799–804.

    PubMed  Google Scholar 

  18. Datta J, Palmer MJ, Tanton C, Gibson LJ, Jones KG, et al. Prevalence of infertility and help seeking among 15 000 women and men. Hum Reprod. 2016;31(9):2108–18. https://doi.org/10.1093/humrep/dew123. Epub 2016 Jun 30.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Bayasgalan G, Naranbat D, Tsedmaa B, Tsogmaa B, Sukhee D, et al. Clinical patterns and major causes of infertility in Mongolia. J Obstet Gynaecol Res. 2004;30(5):386–93.

    Article  PubMed  Google Scholar 

  20. Poongothai J, Gopenath TS, Manonayaki S. Genetics of human male infertility. Singap Med J. 2009;50(4):336–47.

    CAS  Google Scholar 

  21. Martinez G, Daniels K, Chandra A. Fertility of men and women aged 15-44 years in the United States: National Survey of Family Growth, 2006-2010. Natl Health Stat Rep. 2012;51:1–28.

    Google Scholar 

  22. Collins HP, Kalisch D. The health of Australia’s males. Health. Australian Institute of Health and Welfare: Canberra; 2011.

    Google Scholar 

  23. Jungwirth A, Giwercman A, Tournaye H, Diemer T, Kopa Z, Dohle G, et al. European association of urology guidelines on male infertility: the 2012 update. Eur Urol. 2012;62:324–32.

    Article  PubMed  Google Scholar 

  24. Barratt C, Bjorndahl L, De Jong C, Lamb D, Martini FO, et al. The diagnosis of male infertility: an analysis of the evidence to support the development of global WHO guidance—challenges and future research opportunities. Hum Reprod Update. 2017;23(6):660–80.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Stouffs K, Seneca S, Lissens W. Genetic causes of male infertility. Ann Endocrinol (Paris). 2014;75(2):109–11. https://doi.org/10.1016/j.ando.2014.03.004. Epub 2014 Apr 24.

    Article  Google Scholar 

  26. Krausz C, Escamilla AR, Chianese C. Genetics of male infertility: from research to clinic. Reproduction. 2015;150(5):R159–74. https://doi.org/10.1530/REP-15-0261.

    Article  CAS  PubMed  Google Scholar 

  27. Chandley AC. Chromosome anomalies and Y chromosome microdeletions as causal factors in male infertility. Hum Reprod. 1998;13(Suppl 1):45–50.

    Article  CAS  PubMed  Google Scholar 

  28. Samli H, Samli MM, Solak M, Imirzalioglu N. Genetic anomalies detected in patients with non-obstructive azoospermia and oligozoospermia. Arch Androl. 2006;52(4):263–7.

    Article  CAS  PubMed  Google Scholar 

  29. Wosnitzer M, Goldstein M, Hardy MP. Review of Azoospermia. Spermatogenesis. 2014;4:e28218. eCollection 2014.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Lee JY, Dada R, Sabanegh E, Carpi A, Agarwal A. Role of genetics in azoospermia. Urology. 2011;77(3):598–601. https://doi.org/10.1016/j.urology.2010.10.001. Epub 2010 Dec 31.

    Article  PubMed  Google Scholar 

  31. Palermo GD, Colombero LT, Hariprashad JJ, Schlegel PN, Rosenwaks Z. Chromosome analysis of epididymal and testicular sperm in azoospermic patients undergoing ICSI. Hum Reprod. 2002;17(3):570–5.

    Article  PubMed  Google Scholar 

  32. Mackic-Djurovic M, Hasic S, Kiseljakovic E, Rukavina D, Ibrulj S. Cytogenetic abnormalities found in patients with reproductive problems. Med Arch. 2017;71(6):396–9. https://doi.org/10.5455/medarh.2017.71.396-399.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Johnson MD. Genetic risks of intracytoplasmic sperm injection in the treatment of male infertility: recommendations for genetic counseling and screening. Fertil Steril. 1998;70(3):397–411.

    Article  CAS  PubMed  Google Scholar 

  34. Vincent MC, Daudin M, De MP, Massat G, Mieusset R, et al. Cytogenetic investigations of infertile men with low sperm counts: a 25-year experience. J Androl. 2002;23(1):18–22; discussion 44-5.

    Article  PubMed  Google Scholar 

  35. Nagvenkar P, Desai K, Hinduja I, Zaveri K. Chromosomal studies in infertile men with oligozoospermia & non-obstructive azoospermia. Indian J Med Res. 2005;122(1):34–42.

    PubMed  Google Scholar 

  36. Riccaboni A, Lalatta F, Caliari I, Bonetti S, Somigliana E, Ragni G. Genetic screening in 2,710 infertile candidate couples for assisted reproductive techniques: results of application of Italian guidelines for the appropriate use of genetic tests. Fertil Steril. 2008;89(4):800–8. Epub 2007 Aug 6.

    Article  PubMed  Google Scholar 

  37. Mafra FA, Christofolini DM, Bianco B, Gava MM, Glina S, et al. Chromosomal and molecular abnormalities in a group of Brazilian infertile men with severe oligozoospermia or non-obstructive azoospermia attending an infertility service. Int Braz J Urol. 2011;37(2):244–50; discussion 250-1.

    Article  PubMed  Google Scholar 

  38. Arafa M, Majzoub A, AlSaid S, Ansari W, Al Ansari A, Elbardisi Y, Elbardisi H. Chromosomal abnormalities in infertile men with azoospermia and severe oligozoospermia in Qatar and their association with sperm retrieval intracytoplasmic sperm injection outcomes. Arab J Urol. 2018;16(1):132–9.

    Article  PubMed  Google Scholar 

  39. Punab M, Poolamets O, Paju P, Vihljajev V, Pomm K. et. al. Causes of male infertility: a 9-year prospective monocentre study on 1737 patients with reduced total sperm counts. Hum Reprod. 2017;32(1):18–31. Epub 2016 Nov 17.

    CAS  PubMed  Google Scholar 

  40. Xie C, Chen X, Liu Y, Wu Z, Ping P. Multicenter study of genetic abnormalities associated with severe oligospermia and non-obstructive azoospermia. J Int Med Res. 2018;46(1):107–14. https://doi.org/10.1177/0300060517718771. Epub 2017 Jul 21.

    Article  CAS  PubMed  Google Scholar 

  41. Patel B, Parets S, Akana M, Kellogg G, Jansen M, et al. Comprehensive genetic testing for female and male infertility using next-generation sequencing. J Assist Reprod Genet. 2018;35(8):1489–96. https://doi.org/10.1007/s10815-018-1204-7. Epub 2018 May 19.

    Article  PubMed  PubMed Central  Google Scholar 

  42. De Braekeleer M, Dao TN. Cytogenetic studies in male infertility: a review. Hum Reprod. 1991;6(2):245–50.

    Article  PubMed  Google Scholar 

  43. Pieters J, Kooper A, Feuth T, Smits A. Considering factors affecting the parental decision to abort after a prenatal diagnosis of a sex chromosome abnormality. Genet Med. 2012;14:558–9.

    Article  PubMed  Google Scholar 

  44. Forti G, Corona G, Vignozzi L, Krausz C, Maggi M. Klinefelter’s syndrome: a clinical and therapeutical update. Sex Dev. 2010;4(4–5):249–58. https://doi.org/10.1159/000316604. Epub 2010 Jul 21.

    Article  CAS  PubMed  Google Scholar 

  45. Sørensen K, Nielsen J, Jacobsen P, Rolle T. The 48,XXYY syndrome. J Ment Defic Res. 1978;22(3):197–205.

    PubMed  Google Scholar 

  46. Kleczkowska A, Fryns JP, Van den Berghe H. X-chromosome polysomy in the male. The Leuven experience 1966-1987. Hum Genet. 1988;80(1):16–22.

    Article  CAS  PubMed  Google Scholar 

  47. Bojesen A, Juul S, Gravholt CH. Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study. J Clin Endocrinol Metab. 2003;88(2):622–6.

    Article  CAS  PubMed  Google Scholar 

  48. Coffee B, Keith K, Albizua I, Malone T, Mowrey J, et al. Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. Am J Hum Genet. 2009;85(4):503–14. https://doi.org/10.1016/j.ajhg.2009.09.007.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Corona G, Pizzocaro A, Lanfranco F, Garolla A, Pelliccione F, et al. Sperm recovery and ICSI outcomes in Klinefelter syndrome: a systematic review and meta-analysis. Hum Reprod Update. 2017;23(3):265–75. https://doi.org/10.1093/humupd/dmx008.

    Article  CAS  PubMed  Google Scholar 

  50. Krausz C, Hoefsloot L, Simoni M, Tüttelmann F, European Academy of Andrology; European Molecular Genetics Quality Network. EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013. Andrology. 2014;2(1):5–19. https://doi.org/10.1111/j.2047-2927.2013.00173.x.

    Article  CAS  PubMed  Google Scholar 

  51. Colaco S, Modi D. Genetics of the human Y chromosome and its association with male infertility. Reprod Biol Endocrinol. 2018;16(1):14. https://doi.org/10.1186/s12958-018-0330-5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Yousefi-Razin E, Nasiri MJ, Omrani MD. Frequency of Y chromosome microdeletions among Iranian infertile men with Azoospermia and severe Oligozoospermia: a meta-analysis. J Reprod Infertil. 2016;17(4):208–12.

    PubMed  PubMed Central  Google Scholar 

  53. Johnson M, Raheem A, De Luca F, Hallerstrom M, Zainal Y, et al. An analysis of the frequency of Y-chromosome microdeletions and the determination of a threshold sperm concentration for genetic testing in infertile men. BJU Int. 2019;123(2):367–72. https://doi.org/10.1111/bju.14521. Epub 2018 Sep 9.

    Article  CAS  PubMed  Google Scholar 

  54. Chellat D, Rezgoune ML, McElreavey K, Kherouatou N, Benbouhadja S, et al. First study of microdeletions in the Y chromosome of Algerian infertile men with idiopathic oligo- or azoospermia. Urol Int. 2013;90(4):455–9. https://doi.org/10.1159/000347046. Epub 2013 Mar 16.

    Article  PubMed  Google Scholar 

  55. Kim MJ, Choi HW, Park SY, Song IO, Seo JT, Lee HS. Molecular and cytogenetic studies of 101 infertile men with microdeletions of Y chromosome in 1,306 infertile Korean men. J Assist Reprod Genet. 2012;29(6):539–46. https://doi.org/10.1007/s10815-012-9748-4. Epub 2012 Mar 29.

    Article  PubMed  PubMed Central  Google Scholar 

  56. Rejeb I, M’rad R, Maazoul F, Trabelsi M, Ben Jemaa L, et al. Y chromosome microdeletions in Tunisian infertile males. Pathol Biol (Paris). 2008;56(3):111–5. Epub 2007 Nov 26.

    Article  CAS  Google Scholar 

  57. Sen S, Pasi AR, Dada R, Shamsi MB, Modi D. Y chromosome microdeletions in infertile men: prevalence, phenotypes and screening markers for the Indian population. J Assist Reprod Genet. 2013;30(3):413–22. https://doi.org/10.1007/s10815-013-9933-0. Epub 2013 Jan 24.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Hinch AG, Altemose N, Noor N, Donnelly P, Myers SR. Recombination in the human Pseudoautosomal region PAR1. PLoS Genet. 2014;10(7):e1004503. https://doi.org/10.1371/journal.pgen.1004503. eCollection 2014 Jul.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Bansal SK, Jaiswal D, Gupta N, Singh K, Dada R, et al. Gr/gr deletions on Y-chromosome correlate with male infertility: an original study, meta-analyses, and trial sequential analyses. Sci Rep. 2016;6:19798. https://doi.org/10.1038/srep19798.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Liou TG, Rubenstein RC. Carrier screening, incidence of cystic fibrosis, and difficult decisions. JAMA. 2009;302(23):2595–6. https://doi.org/10.1001/jama.2009.1865.

    Article  CAS  PubMed  Google Scholar 

  61. Krausz C, Cioppi F, Riera-Escamilla A. Testing for genetic contributions to infertility: potential clinical impact. Expert Rev Mol Diagn. 2018;18(4):331–46. https://doi.org/10.1080/14737159.2018.1453358. Epub 2018 Mar 22.

    Article  CAS  PubMed  Google Scholar 

  62. Lissens W, Mercier B, Tournaye H, Bonduelle M, Férec C, et al. Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entities. Hum Reprod. 1996;11(Suppl 4):55–78; discussion 79-80.

    Article  PubMed  Google Scholar 

  63. Ferlin A, Raicu F, Gatta V, Zuccarello D, Palka G, Foresta C. Male infertility: role of genetic background. Reprod Biomed Online. 2007;14(6):734–45.

    Article  CAS  PubMed  Google Scholar 

  64. Bareil C, Guittard C, Altieri JP, Templin C, Claustres M, des Georges M. Comprehensive and rapid genotyping of mutations and haplotypes in congenital bilateral absence of the vas deferens and other cystic fibrosis transmembrane conductance regulator-related disorders. J Mol Diagn. 2007;9(5):582–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Singh R, Hamada AJ, Bukavina L, Agarwal A. Physical deformities relevant to male infertility. Nat Rev Urol. 2012;9(3):156–74. https://doi.org/10.1038/nrurol.2012.11.

    Article  CAS  PubMed  Google Scholar 

  66. Estivill X, Bancells C, Ramos C. Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations. The Biomed CF Mutation Analysis Consortium. Hum Mutat. 1997;10(2):135–54.

    Article  CAS  PubMed  Google Scholar 

  67. Patrizio P, Leonard DG. Mutations of the cystic fibrosis gene and congenital absence of the vas deferens. Results Probl Cell Differ. 2000;28:175–86.

    Article  CAS  PubMed  Google Scholar 

  68. Kuligowska E, Fenlon HM. Transrectal US in male infertility: spectrum of findings and role in patient care. Radiology. 1998;207(1):173–81.

    Article  CAS  PubMed  Google Scholar 

  69. Shapiro E, Goldfarb DA, Ritchey ML. The congenital and acquired solitary kidney. Rev Urol. 2003;5:2–8.

    PubMed  PubMed Central  Google Scholar 

  70. Donohue RE, Fauver HE. Unilateral absence of the vas deferens. A useful clinical sign. JAMA. 1989;261(8):1180–2.

    Article  CAS  PubMed  Google Scholar 

  71. McCallum T, Milunsky J, Munarriz R, Carson R, Sadeghi-Nejad H, Oates R. Unilateral renal agenesis associated with congenital bilateral absence of the vas deferens: phenotypic findings and genetic considerations. Hum Reprod. 2001;16(2):282–8.

    Article  CAS  PubMed  Google Scholar 

  72. Jacobs PA, Melville M, Ratcliffe S, Keay AJ, Syme J. A cytogenetic survey of 11,680 newborn infants. Ann Hum Genet. 1974;37(4):359–76.

    Article  CAS  PubMed  Google Scholar 

  73. Kim IW, Khadilkar AC, Ko EY, Sabanegh ES Jr. 47,XYY Syndrome and Male Infertility. Rev Urol. 2013;15(4):188–96.

    PubMed  PubMed Central  Google Scholar 

  74. Children and young adults with sex chromosome aneuploidy-- follow-up, clinical and molecular studies. Minaki, Ontario, Canada, June 7-10, 1989. Birth Defects Orig Artic Ser. 1990;26(4):1–304.

    Google Scholar 

  75. Stochholm K, Juul S, Gravholt CH. Diagnosis and mortality in 47,XYY persons: a registry study. Orphanet J Rare Dis. 2010;5:15. https://doi.org/10.1186/1750-1172-5-15.

    Article  PubMed  PubMed Central  Google Scholar 

  76. Borjian Boroujeni P, Sabbaghian M, Vosough Dizaji A, Zarei Moradi S, Almadani N, et al. Clinical aspects of infertile 47,XYY patients: a retrospective study. Hum Fertil (Camb). 2017:1–6. https://doi.org/10.1080/14647273.2017.1353143.

    Article  PubMed  Google Scholar 

  77. El-Dahtory F, Elsheikha HM. Male infertility related to an aberrant karyotype, 47,XYY: four case reports. Cases J. 2009;2(1):28. https://doi.org/10.1186/1757-1626-2-28.

    Article  PubMed  PubMed Central  Google Scholar 

  78. de la Chapelle A. Nature and origin of males with XX sex chromosomes. Am J Hum Genet. 1972;24:71–105.

    PubMed  PubMed Central  Google Scholar 

  79. Rajender S, Rajani V, Gupta NJ, Chakravarty B, Singh L, Thangaraj K. SRY-negative 46,XX male with normal genitals, complete masculinization and infertility. Mol Hum Reprod. 2006;12:341–6. https://doi.org/10.1093/molehr/gal030.

    Article  CAS  PubMed  Google Scholar 

  80. Majzoub A, Arafa M, Starks C, Elbardisi H, Al Said S, Sabanegh E. 46 XX karyotype during male fertility evaluation; case series and literature review. Asian J Androl. 2017;19(2):168–72. https://doi.org/10.4103/1008-682X.181224.

    Article  CAS  PubMed  Google Scholar 

  81. Akinsal EC, Baydilli N, Demirtas A, Saatci C, Ekmekcioglu O. Ten cases with 46,XX testicular disorder of sex development: single center experience. Int Braz J Urol. 2017;43(4):770–5. https://doi.org/10.1590/S1677-5538.IBJU.2016.0505.

    Article  PubMed  PubMed Central  Google Scholar 

  82. Mohammadpour Lashkari F, Totonchi M, Zamanian MR, Mansouri Z, Sadighi Gilani MA, et al. 46,XX males: a case series based on clinical and genetics evaluation. Andrologia. 2017;49(7) https://doi.org/10.1111/and.12710. Epub 2016 Nov 24.

    Article  CAS  Google Scholar 

  83. Chen T, Tian L, Wu F, Xuan X, Ma G, et al. Clinical and genetic analysis in males with 46,XX disorders of sex development: a reproductive centre experience of 144 cases. Andrologia. 2019:e13232. https://doi.org/10.1111/and.13232.

    Article  PubMed  CAS  Google Scholar 

  84. Topaloglu AK, Kotan LD. Genetics of hypogonadotropic hypogonadism. Endocr Dev. 2016;29:36–49. https://doi.org/10.1159/000438841. Epub 2015 Dec 17.

    Article  CAS  PubMed  Google Scholar 

  85. Topaloğlu AK. Update on the genetics of idiopathic hypogonadotropic hypogonadism. J Clin Res Pediatr Endocrinol. 2017;9(Suppl 2):113–22. https://doi.org/10.4274/jcrpe.2017.S010. Epub 2017 Dec 27.

    Article  PubMed  PubMed Central  Google Scholar 

  86. Boehm U, Bouloux PM, Dattani MT, de Roux N, Dodé C, et al. Expert consensus document: European consensus statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment. Nat Rev Endocrinol. 2015;11(9):547–64. https://doi.org/10.1038/nrendo.2015.112. Epub 2015 Jul 21.

    Article  PubMed  Google Scholar 

  87. Fechner A, Fong S, McGovern P. A review of Kallmann syndrome: genetics, pathophysiology, and clinical management. Obstet Gynecol Surv. 2008;63(3):189–94. https://doi.org/10.1097/OGX.0b013e3181641278.

    Article  PubMed  Google Scholar 

  88. Abujbara MA, Hamamy HA, Jarrah NS, Shegem NS, Ajlouni KM. Clinical and inheritance profiles of Kallmann syndrome in Jordan. Reprod Health. 2004 Oct 24;1(1):5.

    Article  PubMed  PubMed Central  Google Scholar 

  89. Layman LC. Genetics of human hypogonadotropic hypogonadism. Am J Med Genet. 1999;89(4):240–8.

    Article  CAS  PubMed  Google Scholar 

  90. Martin RH. Cytogenetic determinants of male fertility. Hum Reprod Update. 2008;14(4):379–90. https://doi.org/10.1093/humupd/dmn017. Epub 2008 Jun 4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  91. Mayeur A, Ahdad N, Hesters L, Brisset S, Romana S, et al. Chromosomal translocations and semen quality: a study on 144 male translocation carriers. Reprod Biomed Online. 2019;38(1):46–55. https://doi.org/10.1016/j.rbmo.2018.10.003. Epub 2018 Nov 13.

    Article  CAS  PubMed  Google Scholar 

  92. Antonelli A, Gandini L, Petrinelli P, Marcucci L, et al. Chromosomal alterations and male infertility. J Endocrinol Investig. 2000;23(10):677–83.

    Article  CAS  Google Scholar 

  93. Mau-Holzmann UA. Somatic chromosomal abnormalities in infertile men and women. Cytogenet Genome Res. 2005;111(3–4):317–36.

    Article  CAS  PubMed  Google Scholar 

  94. García-Rodríguez A, Gosálvez J, Agarwal A, Roy R, Johnston S. DNA damage and repair in human reproductive cells. Int J Mol Sci. 2018;20(1). pii: E31) https://doi.org/10.3390/ijms20010031.

    Article  PubMed Central  CAS  Google Scholar 

  95. Kim SS, Jung SC, Kim HJ, Moon HR, Lee JS. Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases. J Korean Med Sci. 1999;14(4):373–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  96. Balasar Ö, Zamani AG, Balasar M, Acar H. Male infertility associated with de novo pericentric inversion of chromosome 1. Turk J Urol. 2017;43(4):560–2. https://doi.org/10.5152/tud.2017.79346. Epub 2017 Dec 1.

    Article  PubMed  PubMed Central  Google Scholar 

  97. Teo SH, Tan M, Knight L, Yeo SH, Ng I. Pericentric inversion 9--incidence and clinical significance. Ann Acad Med Singap. 1995;24(2):302–4.

    CAS  PubMed  Google Scholar 

  98. Cotter PD, Babu A, McCurdy LD, Caggana M, Willner JP, Desnick RJ. Homozygosity for pericentric inversions of chromosome 9. Prenatal diagnosis of two cases. Ann Genet. 1997;40(4):222–6.

    CAS  PubMed  Google Scholar 

  99. Kirkpatrick G, Chow V, Ma S. Meiotic recombination, synapsis, meiotic inactivation and sperm aneuploidy in a chromosome 1 inversion carrier. Reprod Biomed Online. 2012;24(1):91–100. https://doi.org/10.1016/j.rbmo.2011.09.013. Epub 2011 Oct 7.

    Article  CAS  PubMed  Google Scholar 

  100. Gardner RJM, Sutherland GR. Chromosome abnormalities and genetic counseling. Am J Hum Genet. 1997;60(6):1567–8.

    Google Scholar 

  101. Cheong KF, Knight LA, Tan M, Ng IS. Variants of chromosome 9 in phenotypically normal individuals. Ann Acad Med Singap. 1997;26(3):312–4.

    CAS  PubMed  Google Scholar 

  102. Ait-Allah A, Ming PM, Salem H, Reece A. The clinical importance of pericentric inversion of chromosome 9 in prenatal diagnosis. J Mat Fetal Invest. 1997;7:126–8.

    Google Scholar 

  103. Guttenbach M, Engel W, Schmid M. Analysis of structural and numerical chromosome abnormalities in sperm of normal men and carriers of constitutional chromosome aberrations. A review. Hum Genet. 1997;100(1):1–21.

    Article  CAS  PubMed  Google Scholar 

  104. Dana M, Stoian V. Association of pericentric inversion of chromosome 9 and infertility in romanian population. Maedica (Buchar). 2012;7(1):25–9.

    Google Scholar 

  105. Mozdarani H, Meybodi AM, Karimi H. Impact of pericentric inversion of Chromosome 9 [inv (9) (p11q12)] on infertility. Indian J Hum Genet. 2007;13(1):26–9. https://doi.org/10.4103/0971-6866.32031.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  106. Al-Achkar W, Wafa A, Moassass F. Cytogenetic abnormalities and Y-chromosome microdeletions in infertile Syrian males. Biomed Rep. 2013;1(2):275–9. Epub 2012 Nov 21.

    Article  CAS  PubMed  Google Scholar 

  107. Sasagawa I, Ishigooka M, Kubota Y, Tomaru M, Hashimoto T, Nakada T. Pericentric inversion of chromosome 9 in infertile men. Int Urol Nephrol. 1998;30(2):203–7.

    Article  CAS  PubMed  Google Scholar 

  108. Foresta C, Ferlin A, Gianaroli L, Dallapiccola B. Guidelines for the appropriate use of genetic tests in infertile couples. Eur J Hum Genet. 2002;10(5):303–12.

    Article  PubMed  Google Scholar 

  109. Okutman O, Rhouma MB, Benkhalifa M, Muller J, Viville S. Genetic evaluation of patients with non-syndromic male infertility. J Assist Reprod Genet. 2018;35(11):1939–51. https://doi.org/10.1007/s10815-018-1301-7. Epub 2018 Sep 26.

    Article  PubMed  PubMed Central  Google Scholar 

  110. Van Steirteghem A, Bonduelle M, Devroey P, Liebaers I. Follow-up of children born after ICSI. Hum Reprod Update. 2002;8(2):111–6.

    Article  PubMed  Google Scholar 

  111. Honig SC, Lipshultz LI, Jarow J. Significant medical pathology uncovered by a comprehensive male infertility evaluation. Fertil Steril. 1994;62(5):1028–34.

    Article  CAS  PubMed  Google Scholar 

  112. Kolettis PN, Sabanegh ES. Significant medical pathology discovered during a male infertility evaluation. J Urol. 2001;166(1):178–80.

    Article  CAS  PubMed  Google Scholar 

  113. Jarow J, Sigman M, Kolettis PN, et al. The optimal evaluation of the infertile male: best practice statement reviewed and validity confirmed 2011. Available online: https://www.auanet.org/education/guidelines/male-infertility-d.cfm

  114. Hotaling J, Carrell DT. Clinical genetic testing for male factor infertility: current applications and future directions. Andrology. 2014;2(3):339–50. https://doi.org/10.1111/j.2047-2927.2014.00200.x. Epub 2014 Apr 7.

    Article  CAS  PubMed  Google Scholar 

  115. Carrell DT, Emery BR. Use of automated imaging and analysis technology for the detection of aneuploidy in human sperm. Fertil Steril. 2008;90(2):434–7. Epub 2007 Oct 23.

    Article  PubMed  Google Scholar 

  116. Khurana KK, Baker K, Gao T, Sabanegh ES Jr. The economic burden of genetic tests for the infertile male: a pilot algorithm to improve test predictive value. J Urol. 2014;191(4):1066–71. https://doi.org/10.1016/j.juro.2013.10.069. Epub 2013 Oct 23.

    Article  PubMed  Google Scholar 

  117. Ballantyne A, Goold I, Pearn A, WHO Human Genetics Programme. Medical genetic services in developing countries : the ethical, legal and social implications of genetic testing and screening. Geneva: World Health Organization; 2006. http://www.who.int/iris/handle/10665/43288

    Google Scholar 

  118. Thong MK, See-Toh Y, Hassan J, Ali J. Medical genetics in developing countries in the Asia-Pacific region: challenges and opportunities. Genet Med. 2018;20(10):1114–21. https://doi.org/10.1038/s41436-018-0135-0. Epub 2018 Aug 10.

    Article  PubMed  Google Scholar 

  119. Thong MK. Birth defects registries in the genomics era: challenges and opportunities for developing countries. Front Pediatr. 2014;2(60) https://doi.org/10.3389/fped.2014.00060.eCollection2014.

  120. Winters BR, Walsh TJ. The epidemiology of male infertility. Urol Clin North Am. 2014;41(1):195–204. https://doi.org/10.1016/j.ucl.2013.08.006. Epub 2013 Sep 13.

    Article  PubMed  Google Scholar 

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Martinez, M.P., Elbardisi, H., Majzoub, A., Arafa, M. (2020). Epidemiology of Genetic Disorders in Male Infertility. In: Arafa, M., Elbardisi, H., Majzoub, A., Agarwal, A. (eds) Genetics of Male Infertility. Springer, Cham. https://doi.org/10.1007/978-3-030-37972-8_5

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