BibTex RIS Kaynak Göster

Nonobstruktif Azoospermik ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler

Yıl 2005, Cilt: 6 Sayı: 1, 7 - 11, 01.04.2005

Öz

Kaynakça

  • de Kretser DM. Male infertility. Lancet, 1997; 349:787-90.
  • Chandley A. Chromosome anomalies and Y chromosome microdeletions as casual factors in male infertility. Hum. Reprod, 1998; 13, 45-50.
  • Koulischer L, Schoysman R. Chromosomes and human infertility. I. Mitotic and meiotic chromosome stıdies in 202 consecutive male patients. Clin. Genet, 1974; 5:116-26.
  • Vannn Assche E, Bonduelle M, Tournaye H, et al. Cytogenetics of infertile men . In: Steirteghem AV, Devroey P, and Liebaers I, editors. Genetics and Assisted Human Conception. Hum Reprod, 1996; (11) 4:1-24.
  • Chandley A.C. Chromosomal basis of human infertility. Br Med Bull, 1979; 35(18):1-186.
  • Chiang, H. S., Liu, C.H., Tzeng, C. R., et al. Surgical and pathologic observations of epididymal tubules during microscopic epididymal sperm aspiration for intracytoplasmic sperm injection. Journal of Formos Medicine Association, 1998; 97, 838-844.
  • Brandriff B, Gordon L, Ashworth L, et al., Chromosomes of human sperm: variability among normal individuals. Hum Genet, 1985; 70, 18–24.
  • Kamiguchi Y, Mikamo K. An improved efficient method for analyzing human sperm chromosomes using zona-free hamster ova. Am J Hum Genet, 1986; 38, 724–740.
  • Martin RH, Rademaker AW, Hildebrand K, et al. Variation in the frequency and type of sperm chromosomal abnormalities among normal men. Hum Genet, 1987, 77, 108–114.
  • Chandley AC, Gosden JR, Hargreave TB, et al. Deleted Yq in the sterile son of a man with a satellited Y chromosome (Yqs). Journal of Medicinal Genetics, 1989; 26, 145.
  • Chandley AC, Coke HJ. Human male infertility-Y- linked genes and spermatogenesis. Human Molecular Genetics, 1994; 3, 1449-1452.
  • Palermo G, Joris H, Devroey P, et al. Pregnancies after intracytoplasmic sperm injection of single spermatozoon into an oocyte. Lancet, 1992; 340:17-18.
  • Cummins JM, Jequier AM. Treating male infertility needs more clinical andrology, not less.Hum Reprod, 1994; 9:1214-9.
  • Bhasin S, DeKretser DM, Baker HWG. Clinical review 64, pathophsiology and natural history of male infertility. J Clin Endocrinol Metab, 1994; 79:1525-9.
  • Kleiman SE, Yogev L, Gamzu R, et al. Genetic evaluation of infertile men. Hum Reprod, 1999; (14)1:33-38.
  • Peschka B, Leygraaf J, Van der Ven K, et al. Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection. Hum Reprod. 1999 Sep;14(9):2257-63.
  • Egozcue S, Blanco J, Vendrell JM, et al. Human male infertility: chromosome anomalies, meiotic disorders, abnormal spermatozoa and recurrent abortion. Hum Reprod Update. 2000 Jan-Feb;6(1):93-105.
  • Abramsson L, Beckman G, Duchek M, et al. Chromosomal aberrations and male infertility. J Urol. 1982 Jul;128(1):52-3.
  • Kjessler B. Chromosomal constituition and male reproductive failure. In Mancini, R.E. and Martini, L. (eds) Male fertility and sterility. Academic Press, New York, USA, 231-247, 1974.
  • Basaran S, Engur A, Aytan M, et al. The Results of Cytogenetic Analysis with Regard to Intracytoplasmic Sperm Injection in Males, Famales and Fetuses. Fetal Diagn Ther 2004;19:313-318.
  • Palermo GD, Colombero LT, Harisprashad JJ, et al. Chromosome analysis of epydidymal and testicular sperm in azoospermic patients undergoing ICSI. Hum Reprod, 2002;(17)3:570-575.
  • Lee S, Kim NK, Kim HJ, et al. Genetic analysis of three polymorphic sites of the luteinizing hormone beta-subunit gene in infertile Korean men with nonobstructive azoospermia. Fertil Steril, 2003; 79(3): 517-21.
  • Rivas F, Garcia-Esquivel L, Diaz M, et al. Cytogenetic evaluation of 163 azoospermics. Journale de Génétique Humaine, 1987; 35, 291-298.
  • Bourrouillou G, Dastugue N, Colombies P. Chromosome studies in 952 males with a sperm count below 10 million/ml. Human Genetics, 1985; 71, 366-367.
  • Retief AE, Van Zyl JA, Menkveld R, Fox M F, et al. Chromosome studies in 496 infertile males with a sperm count below 10 million/ml. Human Genetics, 1984; 66,162-164.
  • De Braekeleer M, Dao T. Cytogenetics studies in male infertility: a review.Hum Reprod, 1991; 6.245- 250.
  • Penna Videau S, Araujo H, Ballesta F, et al. Chromosomal Abnormalities and Polymorphisms in Infertile Men. Archives of Andrology, 2001; 46:205- 210.
  • KCourt-Brown WM, Jacobs P, Brunton M. Chromosome studies on randomly chosen men and women. Lancet, 1965;561-562.
  • Chandley AC, Mc Beath S, Speed RM. Pericentric inversion in human chromosome 1and the risk for male sterility. J Med Genet, 1987; 24:325-34.
  • Colls P, Blanco J, Martınez-Pasarell O, et al. Chromosome segregation in a man heterozygous for a pericentic inversion, inv(9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescent in situ hybridization. Hum Genet, 1997; 99:761-765.
  • Huynh T, Mollard R, Trounson A. Selected genetic factors associated with male infertility. Hum Reprod Update, 2002; (8):2,183-198.
  • Okada H, Fujioka H, Tatsumi N, et al. Klinefelter’s syndrome in the male infertility clinic. Hum Reprod,1999;14:946-952.
  • Dohle GR, Halley DJJ, Van Hemel JO, et al. Genetic risk factors in infertile men with severe oligozoospermia and azoospermia. Hum Reprod, 2002;(17):1,13-16.
  • WHO (1992) World Health Organisation laboratory manual for the examination of human semen and sperm-cervical mucus interaction. Cambridge University Press, Cambridge, UK.

Nonobstruktif Azoospermik ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler

Yıl 2005, Cilt: 6 Sayı: 1, 7 - 11, 01.04.2005

Öz

Genetik faktörler erkek infertilitesi nedenleri arasında
önemli bir yer tutmaktadır. Sayısal ve yapısal
kromozomal düzensizliklere, sebebi bilinmeyen
oligozoospermik ve azoospermik olgularda sık rastlanmaktadır.
Bu çalışmada 1995-2005 yılları arasında
infertilite kıliniğine başvuran 383 azoospermik ve 436
şiddetli oligozoospermik toplam 819 Türk erkek incelemeye
alındı. Bir ay ara ile iki kez spermogram ve basal
hormon profilleri (FSH-Testosterone) çalışıldı. Tüm olguların
karyogram analizleri yapıldı.
İncelenen 383 azoospermik olgunun 47(%12,3) tanesinde,
436 oligozoospermik olgunun 20(%4,6) tanesinde
kromozomal düzensizlik tesbit edilmiştir. Azoospermik
olgularda tesbit edilen kromozomal düzensizliklerin
9(%19,1) tanesi otosomal ve 38(%80,9) tanesi gonozomal
kromozomlara ait bulunmuştur. Oligozoospermik olgularda
ise tespit edilen kromozomal düzensizliklerin 8(%40)
tanesi otozomal, 12(%60) tanesi gonozomal kromozomlara
aittir.
Erkekte infertiliteye neden olan genetik nedenlerin belirlenmesi
ve yardımcı üreme teknikleri kullanılarak elde edilecek
bu bireylere ait çocukların taşıyabilecekleri genetik
riskin saptanması amacıyla infertilite kliniğine başvuran
azoospermik, oligozoospermik infertil erkeklerde genetik
danışma verilmesi ve sitogenetik inceleme yapılması
doğru tanının konmasına yardımcı olacaktır.

Kaynakça

  • de Kretser DM. Male infertility. Lancet, 1997; 349:787-90.
  • Chandley A. Chromosome anomalies and Y chromosome microdeletions as casual factors in male infertility. Hum. Reprod, 1998; 13, 45-50.
  • Koulischer L, Schoysman R. Chromosomes and human infertility. I. Mitotic and meiotic chromosome stıdies in 202 consecutive male patients. Clin. Genet, 1974; 5:116-26.
  • Vannn Assche E, Bonduelle M, Tournaye H, et al. Cytogenetics of infertile men . In: Steirteghem AV, Devroey P, and Liebaers I, editors. Genetics and Assisted Human Conception. Hum Reprod, 1996; (11) 4:1-24.
  • Chandley A.C. Chromosomal basis of human infertility. Br Med Bull, 1979; 35(18):1-186.
  • Chiang, H. S., Liu, C.H., Tzeng, C. R., et al. Surgical and pathologic observations of epididymal tubules during microscopic epididymal sperm aspiration for intracytoplasmic sperm injection. Journal of Formos Medicine Association, 1998; 97, 838-844.
  • Brandriff B, Gordon L, Ashworth L, et al., Chromosomes of human sperm: variability among normal individuals. Hum Genet, 1985; 70, 18–24.
  • Kamiguchi Y, Mikamo K. An improved efficient method for analyzing human sperm chromosomes using zona-free hamster ova. Am J Hum Genet, 1986; 38, 724–740.
  • Martin RH, Rademaker AW, Hildebrand K, et al. Variation in the frequency and type of sperm chromosomal abnormalities among normal men. Hum Genet, 1987, 77, 108–114.
  • Chandley AC, Gosden JR, Hargreave TB, et al. Deleted Yq in the sterile son of a man with a satellited Y chromosome (Yqs). Journal of Medicinal Genetics, 1989; 26, 145.
  • Chandley AC, Coke HJ. Human male infertility-Y- linked genes and spermatogenesis. Human Molecular Genetics, 1994; 3, 1449-1452.
  • Palermo G, Joris H, Devroey P, et al. Pregnancies after intracytoplasmic sperm injection of single spermatozoon into an oocyte. Lancet, 1992; 340:17-18.
  • Cummins JM, Jequier AM. Treating male infertility needs more clinical andrology, not less.Hum Reprod, 1994; 9:1214-9.
  • Bhasin S, DeKretser DM, Baker HWG. Clinical review 64, pathophsiology and natural history of male infertility. J Clin Endocrinol Metab, 1994; 79:1525-9.
  • Kleiman SE, Yogev L, Gamzu R, et al. Genetic evaluation of infertile men. Hum Reprod, 1999; (14)1:33-38.
  • Peschka B, Leygraaf J, Van der Ven K, et al. Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection. Hum Reprod. 1999 Sep;14(9):2257-63.
  • Egozcue S, Blanco J, Vendrell JM, et al. Human male infertility: chromosome anomalies, meiotic disorders, abnormal spermatozoa and recurrent abortion. Hum Reprod Update. 2000 Jan-Feb;6(1):93-105.
  • Abramsson L, Beckman G, Duchek M, et al. Chromosomal aberrations and male infertility. J Urol. 1982 Jul;128(1):52-3.
  • Kjessler B. Chromosomal constituition and male reproductive failure. In Mancini, R.E. and Martini, L. (eds) Male fertility and sterility. Academic Press, New York, USA, 231-247, 1974.
  • Basaran S, Engur A, Aytan M, et al. The Results of Cytogenetic Analysis with Regard to Intracytoplasmic Sperm Injection in Males, Famales and Fetuses. Fetal Diagn Ther 2004;19:313-318.
  • Palermo GD, Colombero LT, Harisprashad JJ, et al. Chromosome analysis of epydidymal and testicular sperm in azoospermic patients undergoing ICSI. Hum Reprod, 2002;(17)3:570-575.
  • Lee S, Kim NK, Kim HJ, et al. Genetic analysis of three polymorphic sites of the luteinizing hormone beta-subunit gene in infertile Korean men with nonobstructive azoospermia. Fertil Steril, 2003; 79(3): 517-21.
  • Rivas F, Garcia-Esquivel L, Diaz M, et al. Cytogenetic evaluation of 163 azoospermics. Journale de Génétique Humaine, 1987; 35, 291-298.
  • Bourrouillou G, Dastugue N, Colombies P. Chromosome studies in 952 males with a sperm count below 10 million/ml. Human Genetics, 1985; 71, 366-367.
  • Retief AE, Van Zyl JA, Menkveld R, Fox M F, et al. Chromosome studies in 496 infertile males with a sperm count below 10 million/ml. Human Genetics, 1984; 66,162-164.
  • De Braekeleer M, Dao T. Cytogenetics studies in male infertility: a review.Hum Reprod, 1991; 6.245- 250.
  • Penna Videau S, Araujo H, Ballesta F, et al. Chromosomal Abnormalities and Polymorphisms in Infertile Men. Archives of Andrology, 2001; 46:205- 210.
  • KCourt-Brown WM, Jacobs P, Brunton M. Chromosome studies on randomly chosen men and women. Lancet, 1965;561-562.
  • Chandley AC, Mc Beath S, Speed RM. Pericentric inversion in human chromosome 1and the risk for male sterility. J Med Genet, 1987; 24:325-34.
  • Colls P, Blanco J, Martınez-Pasarell O, et al. Chromosome segregation in a man heterozygous for a pericentic inversion, inv(9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescent in situ hybridization. Hum Genet, 1997; 99:761-765.
  • Huynh T, Mollard R, Trounson A. Selected genetic factors associated with male infertility. Hum Reprod Update, 2002; (8):2,183-198.
  • Okada H, Fujioka H, Tatsumi N, et al. Klinefelter’s syndrome in the male infertility clinic. Hum Reprod,1999;14:946-952.
  • Dohle GR, Halley DJJ, Van Hemel JO, et al. Genetic risk factors in infertile men with severe oligozoospermia and azoospermia. Hum Reprod, 2002;(17):1,13-16.
  • WHO (1992) World Health Organisation laboratory manual for the examination of human semen and sperm-cervical mucus interaction. Cambridge University Press, Cambridge, UK.
Toplam 34 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Makaleler-Araştırma Yazıları
Yazarlar

Hale Şamlı Bu kişi benim

Mustafa Solak Bu kişi benim

Necat İmirzalioğlu Bu kişi benim

M. Murat Şamlı Bu kişi benim

Yayımlanma Tarihi 1 Nisan 2005
Yayımlandığı Sayı Yıl 2005 Cilt: 6 Sayı: 1

Kaynak Göster

APA Şamlı, H., Solak, M., İmirzalioğlu, N., Şamlı, M. . M. . (2005). Nonobstruktif Azoospermik ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler. Kocatepe Tıp Dergisi, 6(1), 7-11. https://doi.org/10.18229/ktd.06989
AMA Şamlı H, Solak M, İmirzalioğlu N, Şamlı MM. Nonobstruktif Azoospermik ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler. KTD. Nisan 2005;6(1):7-11. doi:10.18229/ktd.06989
Chicago Şamlı, Hale, Mustafa Solak, Necat İmirzalioğlu, ve M. Murat Şamlı. “Nonobstruktif Azoospermik Ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler”. Kocatepe Tıp Dergisi 6, sy. 1 (Nisan 2005): 7-11. https://doi.org/10.18229/ktd.06989.
EndNote Şamlı H, Solak M, İmirzalioğlu N, Şamlı MM (01 Nisan 2005) Nonobstruktif Azoospermik ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler. Kocatepe Tıp Dergisi 6 1 7–11.
IEEE H. Şamlı, M. Solak, N. İmirzalioğlu, ve M. . M. . Şamlı, “Nonobstruktif Azoospermik ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler”, KTD, c. 6, sy. 1, ss. 7–11, 2005, doi: 10.18229/ktd.06989.
ISNAD Şamlı, Hale vd. “Nonobstruktif Azoospermik Ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler”. Kocatepe Tıp Dergisi 6/1 (Nisan 2005), 7-11. https://doi.org/10.18229/ktd.06989.
JAMA Şamlı H, Solak M, İmirzalioğlu N, Şamlı MM. Nonobstruktif Azoospermik ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler. KTD. 2005;6:7–11.
MLA Şamlı, Hale vd. “Nonobstruktif Azoospermik Ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler”. Kocatepe Tıp Dergisi, c. 6, sy. 1, 2005, ss. 7-11, doi:10.18229/ktd.06989.
Vancouver Şamlı H, Solak M, İmirzalioğlu N, Şamlı MM. Nonobstruktif Azoospermik ve Şiddetli Oligozoospermik Erkeklerde Saptanan Kromozomal Anomaliler. KTD. 2005;6(1):7-11.

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