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Pregnancy by ICSI and Genetic Counseling in A 47,XYY Karyotype-Couple

Year 2012, Volume: 1 Issue: 1, 46 - 48, 01.04.2012

Abstract

47,XYY syndrome is a sex chromosome aneuploidy with an extra Y chromosome, and these males are phenotypically normal. The syndrome is associated with an increased risk of infertility, cancer and neurological diseases. Here, we report a 47,XYY karyotyped male who has a normal karyotyped baby by intractoplasmic sperm injection ICSI and discuss the importance of genetic counseling process in 47,XYY cases

References

  • Martini E, Geraedts JP, Liebaers I, et al. Constitution
  • of semen samples from XYY and XXY males as
  • analysed by in-situ hybridization. Hum Reprod 1996; 11(8): 1638-43.
  • Athanatos D, Tsakalidis C, Tampakoudis GP, et al. Embryo with XYY syndrome presenting with clubfoot: a case report. Cases J 2009; 2: 8404.
  • Hall H, Hunt P, Hassold T. Meiosis and sex chromosome aneuploidy: how meiotic errors cause aneuploidy; how aneuploidy causes meiotic errors. Curr Opin Genet Dev 2006; 16(3): 323-9.
  • Honma T, Kanegane H, Shima T, Otsubo K, Nomura K, Miyawaki T. Neuroblastoma in an XYY male. Cancer Genet Cytogenet 2006; 168(1): 83-4.
  • El-Dahtory F, Elsheikha HM. Male infertility related to an aberrant karyotype, 47,XYY: four case reports. Cases J 2009; 2(1): 28.
  • Ruud A, Arnesen P, Stray LL, Vildalen S, Vesterhus P. Stimulant medication in 47,XYY syndrome: a report of two cases. Dev Med Child Neurol 2005; 47(8): 559-62.
  • Ross JL, Zeger MP, Kushner H, Zinn AR, Roeltgen DP. An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome. Dev Disabil Res Rev 2009; 15(4): 309-17.
  • Abdel-Razic MM, Abdel-Hamid IA, Elsobky ES. Nonmosaic 47,XYY syndrome presenting with male infertility: case series. Andrologia 2011; DOI: 10.1111/j.1439-0272.2010.01129.x
  • Vicdan K, Akarsu C,Vicdan A, ve ark. Birth of a healthy boy using fresh testicular spermin a patient with Klinefelter syndrome combined with Kartagener syndrome. Fertil Steril 2011; 96(3): 577-9.
  • Palanduz S, Aktan M, Ozturk S, Tutkan G, Cefle K, Pekcelen Y. 47,XYY karyotype in acute myeloid leukemia. Cancer Genet Cytogenet 1998; 106(1): 76-7.
  • Zouli C, Tsametis C, Papadimas I, Goulis DG. A man with 47,XYY karyotype, prolactinoma and a history of first trimester recurrent miscarriages in his wife. Hormones 2011; 10(1): 72-5.
  • Sandlund JT, Raimondi SC. Small noncleaved cell lymphoma in an adolescent with the XYY syndrome. Cancer Genet Cytogenet 1997; 94(2): 88-90.
  • Stochholm K, Juul S, Gravholt CH. Diagnosis and mortality in 47,XYY persons: a registry study. Orphanet J Rare Dis 2010; 5: 15.

47,XYY Karyotipli İnfertil Bir Çiftte ICSI ile Gebelik Eldesi ve Genetik Danışmanlık Süreci

Year 2012, Volume: 1 Issue: 1, 46 - 48, 01.04.2012

Abstract

47,XYY sendromu erkeklerde ekstra Y kromozomunun olduğu bir cinsiyet kromozomu anöploidisidir ve bu erkeklerin büyük bir kısmı fenotipik olarak normal özellik gösterirler. Ancak infertilite, kanser, nörolojik hastalıklar riskinde artma bildirilmiştir. Bu olguda intrasitoplazmik sperm enjeksiyonu ICSI ile normal genotipte bir çocuğa sahip olan 47,XYY genotipli bir vaka sunularak bu tür genotipe sahip bireyler için genetik danışmanlık sürecinin önemi tartışıldı

References

  • Martini E, Geraedts JP, Liebaers I, et al. Constitution
  • of semen samples from XYY and XXY males as
  • analysed by in-situ hybridization. Hum Reprod 1996; 11(8): 1638-43.
  • Athanatos D, Tsakalidis C, Tampakoudis GP, et al. Embryo with XYY syndrome presenting with clubfoot: a case report. Cases J 2009; 2: 8404.
  • Hall H, Hunt P, Hassold T. Meiosis and sex chromosome aneuploidy: how meiotic errors cause aneuploidy; how aneuploidy causes meiotic errors. Curr Opin Genet Dev 2006; 16(3): 323-9.
  • Honma T, Kanegane H, Shima T, Otsubo K, Nomura K, Miyawaki T. Neuroblastoma in an XYY male. Cancer Genet Cytogenet 2006; 168(1): 83-4.
  • El-Dahtory F, Elsheikha HM. Male infertility related to an aberrant karyotype, 47,XYY: four case reports. Cases J 2009; 2(1): 28.
  • Ruud A, Arnesen P, Stray LL, Vildalen S, Vesterhus P. Stimulant medication in 47,XYY syndrome: a report of two cases. Dev Med Child Neurol 2005; 47(8): 559-62.
  • Ross JL, Zeger MP, Kushner H, Zinn AR, Roeltgen DP. An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome. Dev Disabil Res Rev 2009; 15(4): 309-17.
  • Abdel-Razic MM, Abdel-Hamid IA, Elsobky ES. Nonmosaic 47,XYY syndrome presenting with male infertility: case series. Andrologia 2011; DOI: 10.1111/j.1439-0272.2010.01129.x
  • Vicdan K, Akarsu C,Vicdan A, ve ark. Birth of a healthy boy using fresh testicular spermin a patient with Klinefelter syndrome combined with Kartagener syndrome. Fertil Steril 2011; 96(3): 577-9.
  • Palanduz S, Aktan M, Ozturk S, Tutkan G, Cefle K, Pekcelen Y. 47,XYY karyotype in acute myeloid leukemia. Cancer Genet Cytogenet 1998; 106(1): 76-7.
  • Zouli C, Tsametis C, Papadimas I, Goulis DG. A man with 47,XYY karyotype, prolactinoma and a history of first trimester recurrent miscarriages in his wife. Hormones 2011; 10(1): 72-5.
  • Sandlund JT, Raimondi SC. Small noncleaved cell lymphoma in an adolescent with the XYY syndrome. Cancer Genet Cytogenet 1997; 94(2): 88-90.
  • Stochholm K, Juul S, Gravholt CH. Diagnosis and mortality in 47,XYY persons: a registry study. Orphanet J Rare Dis 2010; 5: 15.
There are 15 citations in total.

Details

Primary Language Turkish
Journal Section Research Article
Authors

Murat Kara This is me

Hatice Banu Kumbak Aygün This is me

İbrahim Tekedereli This is me

Publication Date April 1, 2012
Published in Issue Year 2012 Volume: 1 Issue: 1

Cite

APA Kara, M., Aygün, H. B. K., & Tekedereli, İ. (2012). 47,XYY Karyotipli İnfertil Bir Çiftte ICSI ile Gebelik Eldesi ve Genetik Danışmanlık Süreci. Annals of Health Sciences Research, 1(1), 46-48.
AMA Kara M, Aygün HBK, Tekedereli İ. 47,XYY Karyotipli İnfertil Bir Çiftte ICSI ile Gebelik Eldesi ve Genetik Danışmanlık Süreci. Ann Health Sci Res. April 2012;1(1):46-48.
Chicago Kara, Murat, Hatice Banu Kumbak Aygün, and İbrahim Tekedereli. “47,XYY Karyotipli İnfertil Bir Çiftte ICSI Ile Gebelik Eldesi Ve Genetik Danışmanlık Süreci”. Annals of Health Sciences Research 1, no. 1 (April 2012): 46-48.
EndNote Kara M, Aygün HBK, Tekedereli İ (April 1, 2012) 47,XYY Karyotipli İnfertil Bir Çiftte ICSI ile Gebelik Eldesi ve Genetik Danışmanlık Süreci. Annals of Health Sciences Research 1 1 46–48.
IEEE M. Kara, H. B. K. Aygün, and İ. Tekedereli, “47,XYY Karyotipli İnfertil Bir Çiftte ICSI ile Gebelik Eldesi ve Genetik Danışmanlık Süreci”, Ann Health Sci Res, vol. 1, no. 1, pp. 46–48, 2012.
ISNAD Kara, Murat et al. “47,XYY Karyotipli İnfertil Bir Çiftte ICSI Ile Gebelik Eldesi Ve Genetik Danışmanlık Süreci”. Annals of Health Sciences Research 1/1 (April 2012), 46-48.
JAMA Kara M, Aygün HBK, Tekedereli İ. 47,XYY Karyotipli İnfertil Bir Çiftte ICSI ile Gebelik Eldesi ve Genetik Danışmanlık Süreci. Ann Health Sci Res. 2012;1:46–48.
MLA Kara, Murat et al. “47,XYY Karyotipli İnfertil Bir Çiftte ICSI Ile Gebelik Eldesi Ve Genetik Danışmanlık Süreci”. Annals of Health Sciences Research, vol. 1, no. 1, 2012, pp. 46-48.
Vancouver Kara M, Aygün HBK, Tekedereli İ. 47,XYY Karyotipli İnfertil Bir Çiftte ICSI ile Gebelik Eldesi ve Genetik Danışmanlık Süreci. Ann Health Sci Res. 2012;1(1):46-8.