Case Reports

An Infertile Azoospermic Male With 45, X T(Yp;15) Karyotype

Abstract

Objective: 45, X is a very rare condition that usually results from Y/autosomal translocations or insertions. Here we present an infertile azoospermic man who had 45, X t(Yp;15) karyotype and deletion of AZF (azoospermia factor) gene region.
Case report: A 35-year-old infertile azoospermic man with a typical male appearance came for infertility genetic counseling. He was infertile for more than ten years and had short height. High-resolution of metaphase chromosomes of 50 peripheral white blood cells were analyzed for karyotyping. Fluorescence in situ hybridization (FISH) analysis and Polymerase chain reaction (PCR) were done for SRY and AZF gene localization. Karyotyping and FISH analysis revealed 45, X t(Yp;15) karyotype and no mosaicism. More investigation on the Y chromosome revealed no deletion in the SRY region, but AZF a/b/c were deleted. It was revealed that Yp's subtelomeric region but not Yq was translocated to chromosome 15.
Conclusion: This study shows that despite the lack of a complete Y chromosome in this person, the occurrence of secondary male traits is a result of the short arm translocation of the Y chromosome, which contains the (ex-determining region Y) SRY gene. Infertility is also due to the Y chromosomes long arm's deletion containing the AZF gene region.

1. Dati E, Valetto A, Bertini V, Chiocca E, Baroncelli GI, Battini R, et al. 45,X maleness: clinical and cytogenetic features in two patients. Sex Dev 2011; 5: 281-6.
2. Bilen S, Okten A, Karaguzel G, Ikbal M, Aslan Y. A 45 X male patient with 7q distal deletion and rearrangement with SRY gene translocation: a case report. Genet Couns 2013; 24: 299-305.
3. Hsu LY. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases. Am J Med Genet 1994; 53: 108-40.
4. Pinho MJ, Neves R, Costa P, Ferrás C, Sousa M, Alves C, et al. Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report. Hum Reprod 2005; 20: 689-96.
5. Braun-Falco M, Schempp W, Nevinny-Stickel-Hinzpeter C, Köhn FM. Azoospermia due to a unique de novo balanced reciprocal translocation (Y;1) (q12;q25). J Androl 2007; 28: 647-51.
6. Boutouil M, Fetni R, Qu J, Dallaire L, Richer CL, Lemieux N. Fragile site and interstitial telomere repeat sequences at the fusion point of a de novo (Y;13) translocation. Hum Genet 1996; 98: 323-7.
7. Shanske A, Ellison J, Vuguin P, Dowling P, Wasserman E, Heinrich J, et al. Deletion of the pseudoautosomal region in a male with a unique Y;13 translocation and short stature. Am J Med Genet 1999; 82: 34-9.
8. Alves C, Carvalho F, Cremades N, Sousa M, Barros A. Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies. Eur J Hum Genet 2002; 10: 467-74.
9. Borie C, Léger J, Dupuy O, Hassan M, Ledu N, Lebbar A, et al. Translocation (Y;22) resulting in the loss of SHOX and isolated short stature. Am J Med Genet A 2004; 125a: 186-90.
10. Orrico A, Marseglia G, Pescucci C, Cortesi A, Piomboni P, Giansanti A, et al. Molecular Dissection Using Array Comparative Genomic Hybridization and Clinical Evaluation of An Infertile Male Carrier of An Unbalanced Y;21 Translocation: A Case Report and Review of The Literature. Int J Fertil Steril 2016; 9: 581-5.
11. Rey R, Josso N, Racine C. Sexual Differentiation. In Feingold KR, Anawalt B, Boyce A Chrousos G, de Herder WW, Dhatariya K,et al. editors. Endotext [Internet]. South Dartmouth (MA): MDText.com, Inc.; 2000.
12. Vogt PH, Bender U. Human Y chromosome microdeletion analysis by PCR multiplex protocols identifying only clinically relevant AZF microdeletions. Methods Mol Biol 2013; 927: 187-204.
13. Babu A, Verma RS. Human chromosomes : principles and techniques. New York (N.Y.) : McGraw-Hill,1995.
14. McGowan-Jordan J, Hastings R, Moore S. Re: International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts, by T. Liehr. Cytogenet Genome Res 2021; 161: 225-6.
15. Pinkel D, Gray JW, Trask B, van den Engh G, Fuscoe J, van Dekken H. Cytogenetic analysis by in situ hybridization with fluorescently labeled nucleic acid probes. Cold Spring Harb Symp Quant Biol 1986; 51 Pt 1: 151-7.
16. Simoni M, Bakker E, Krausz C. EAA/EMQN best practice guidelines for molecular diagnosis of
y-chromosomal microdeletions. State of the art 2004. Int J Androl 2004; 27: 240-9.
17. Efthymiadou A, Stefanou EG, Chrysis D. 45,X/46,XY mosaicism: a cause of short stature in males. Hormones (Athens) 2012; 11: 501-4.
18. Lee JY, Dada R, Sabanegh E, Carpi A, Agarwal A.
Role of Genetics in Azoospermia. Urology 2011; 77: 598-601.
19. Chen S, Xi Q, Zhang X, Jiang Y, Li L, Liu R, et al. Molecular cytogenetic studies of a male carrier with a unique (Y;14) translocation: Case report. J Clin Lab Anal 2021; 35: e23614.
20. Jia C, Li L, Chen S, Wang X, Liu R, Zhang H. Cytogenetic and molecular characterization of an oligoasthenozoospermia male carrier of an unbalanced Y;22 translocation: A case report. Medicine 2019;
98: e15209.
21. Uehara E, Hattori A, Shima H, Ishiguro A, Abe Y, Ogata T, et al. Unbalanced Y;7 Translocation between Two Low-Similarity Sequences Leading to SRY-Positive 45,X Testicular Disorders of Sex Development. Cytogenet Genome Res 2019; 158: 115-20.
22. Sinclair AH, Berta P, Palmer MS, Hawkins JR, Griffiths BL, Smith MJ, et al. A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif. Nature 1990; 346: 240-4.
23. Foresta C, Moro E, Ferlin A. Y chromosome microdeletions and alterations of spermatogenesis. Endocr Rev 2001; 22: 226-39.
Files
IssueVol 15, No 4 (December 2021) QRcode
SectionCase Reports
DOI https://doi.org/10.18502/jfrh.v15i4.7896
Keywords
Aneuploidy Genetic Translocation Azoospermia Sex-Determining Region Y Protein Fluorescence in situ hybridization

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How to Cite
1.
Abiri M, Hassanlou M, Narimani N, Zamani M, Moeini Z. An Infertile Azoospermic Male With 45, X T(Yp;15) Karyotype. J Family Reprod Health. 2021;15(4):271-274.