Dergiler / Arşiv Kaynak Tarama Dergisi / 2011 / Cilt: 20 - Sayı: 4

Erkek İnfertilitesinin Sitogenetiği

Cytogenetic of Male Infertility

Sayfa
230–245
Yayın Tarihi
2011-12-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Similar chromosome abnormalities are detected in male infertility and as the rate of these abnormalities increase, it was found to reduce sperm count especially in azospermic and oligozoospermic men.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Infertility by definition, is not to get pregnant within one year of regular sexual relationship without protection, affects 15-20% of reproductive age couples.
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Temel Bulgular & Veri:Approximately 30% of infertility cases are male originated.
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Sonuç & Katkı:Similar chromosome abnormalities are detected in male infertility and as the rate of these abnormalities increase, it was found to reduce sperm count especially in azospermic and oligozoospermic men.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:İnfertilite · Erkek infertilitesi · Hormonal düzenleme Spermatogenez

Abstract

Infertility by definition, is not to get pregnant within one year of regular sexual relationship without protection, affects 15-20% of reproductive age couples. Approximately 30% of infertility cases are male originated. Male infertility is caused by endocrine-related genetic defects affecting urogenital system function. These defects adversely affect subsequent spermatogenesis, sexual function, fertility, early embryonic stage of sexual maturation. Autosomal and gonosomal, numerical and structural chromosome abnormalities and related syndromes rank at the top causes of male infertility. Similar chromosome abnormalities are detected in male infertility and as the rate of these abnormalities increase, it was found to reduce sperm count especially in azospermic and oligozoospermic men.

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Bu Makaleye Atıf Yap

ÖZPAK, L., PAZARBAŞI, A. (2011). Erkek İnfertilitesinin Sitogenetiği. Arşiv Kaynak Tarama Dergisi, Cilt: 20 - Sayı: 4, 230–245. https://ajindex.com/articles/466229

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Kaynakça (2)

  1. Mark HFL, Sigman M. Cytogenetics of Male Infertility. In: Medical Cytogenetics, 1st. Edition, New York: Marcel Dekker, 2000; 247-273 Erişim:(http://www.burclab.com/tr/genetik/teknik-bultenler/Y-kromozom-mikrodelesyonlar) Erişim Tarihi: 15.02.2011 3. Demirhan O, Pazarbaşı A, et. al.: The Clinical Effects Of Isochromosome Xq İn Klinefelter Syndrome: Report Of A Case And Rewiew Of Literature, Genetic Counseling, 2009;3: 235- 242 4. Başaran N. Tıbbi genetik, 6. Baskı,
  2. Bilim Teknik Yayınevi, Eskişehir,1996.