Journals / International Archives of Medical Research / 2017 / Cilt: 9 - Sayı: 2

108 patients with sex abnormality; cytogenetic and molecular analysis in Diyarbakır, Turkey

Pages
51–60
Publication Date
2017-12-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The results showed that among 108 patients, 49 were positive for SRY and the remaining negative for SRY.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The relationship between abnormal chromosomal constitution and sex anomalies has been established since the development of cytogenetic and molecular methods.
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Key Findings & Data:In order to investigate the relationship between sex dysplasia and sex-determining region Y (SRY) gene, 108 patients with sexual abnormality were analyzed by cytogenetic and molecular genetic methods.
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Conclusion & Impact:The results showed that among 108 patients, 49 were positive for SRY and the remaining negative for SRY.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Chromosome · Sry gene · sex abnormality

Abstract

The relationship between abnormal chromosomal constitution and sex anomalies has been established since the development of cytogenetic and molecular methods. In order to investigate the relationship between sex dysplasia and sex-determining region Y (SRY) gene, 108 patients with sexual abnormality were analyzed by cytogenetic and molecular genetic methods. SRY gene was amplified by polymerase chain reaction (PCR) and its mutation was detected by direct sequencing. The results showed that among 108 patients, 49 were positive for SRY and the remaining negative for SRY. In the patients positive for SRY genes, with 45, X/46, XY 46, XXY,46,XX karyotype, In the patients negative for SRY, with 46,XY,46, XX karyotype It was concluded that SRY gene is strongly involved in male sex determination, while a sequence of other genes may be taken into account in sexual development. . It is also essential for defining genotypic and phenotypic correlation and understanding the basic mechanism involved in sex determination.

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Cite This Article

ORAL, D., ŞİMŞEK, S., İSİ, H., YÜCE, İ. (2017). 108 patients with sex abnormality; cytogenetic and molecular analysis in Diyarbakır, Turkey. International Archives of Medical Research, Cilt: 9 - Sayı: 2, 51–60. https://ajindex.com/articles/764795

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References (9)

  1. Sinclair AH, Berta P, Palmer MS, Hawkins JR, Griffiths BL, Smith MJ, Foster JW, Frischauf AM, Lovell-Badge R, Goodfellow PN. A gene from the human sex determining region encodes a protein with homology to a conserved DNA binding motif. Nature. 1990;346:240–244. doi: 10.1038/346240a0
  2. Clépet C, Schafer AJ, Sinclair AH, Palmer MS, Lovell- Badge R, Goodfellow PN. The human SRY transcript. Hum Mol Genet. 1993;2:2007–2012 3. Koopman P, Gubbay J, Vivian N, Goodfellow P, Lovell-Badge R. Male development of chromosomally female mice transgenic for Sry. Nature. 1991;351:117–121. doi: 10.1038/351117a0 4. Hawkins JR, Taylor A, Berta P, Levilliers J, Van der Auwera B, Goodfellow PN. Mutational analysis of SRY: nonsense and missense mutations in XY sex reversal. Hum Genet. 1992;88:471–474. doi: 10.1007/BF00215684
  3. Iida T, Nakahori Y, Komaki R, Mori E, Hayashi N, Tsutsumi O, Taketani Y, Nakagome Y. A novel missense mutation in the HMG box of the SRY gene in a patient with XY sex reversal. Hum Mol Genet. 1994;3:1437–1438
  4. Fechner PY, Marcantonio SM, Jaswaney VJ, Stetten G, Goodfellow PN, Migeon CJ, Smith KD, Berkovitz GD, Amrhein JA, Bard PA. The role of the sex determining region Y gene (SRY) in the etiology of 46,XX maleness. J Clin Endocrinol Metab. 1993;76:690–696
  5. Kusz K, Kotecki M, Wojda A, Szarras-Czapnik M, Latos-Bielenska A, Warenik-Szymankiewicz A, Ruszczynska-Wolska A, Jaruzelska J. Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome. J Med Gene. 1999;36:452–456
  6. Affara NA, Ferguson-Smith MA, Magenis RE, Tolmie JL, Boyd E, Cooke A, Jamieson D, Kwok K, Mitchell M, Snadden L. Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes. Nucleic Acids Res. 1987;15:7325–7342
  7. Ferguson-Smith MA. X-Y chromosomal interchange in the aetiology of true hermaphrodism and of XX Klinefelter’s syndrome. Lancet. 1966;2:475–6. doi:10.1016/S0140-6736(66)92778-4
  8. Weil D, Wang I, Dietrich A, Poustka A, Weissenbach J, Petit C. Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness. Nat Genet. 1994;7:414–9. doi:10.1038/ng0794-414 11. de la Chapelle A. The etiology of maleness in XX men. Hum Genet. 1981;58:105–16. doi:10.1007/BF00284157
  9. Boucekkine C, Toublanc JE, Abbas N, Chaabouni S, Ouahid S, Semrouni M, Jaubert F, Toublanc M, McElreavey K, Vilain E, Fellous M. Clinical