نتایج جستجو برای: chromosome microdeletions

تعداد نتایج: 119710  

Journal: :international journal of reproductive biomedicine 0
mohammad ali zaimy seyyed mehdi kalantar mohammad hasan sheikhha tahere jahaninejad hossein pashaiefar jalal ghasemzadeh

background: about 15% of couples have infertility problems which 40% of them are related to the male factors. genetic factors are candidate for about 10% of male infertility conditions. among these, azfa, azfb, azfc and azfd regions on the yq are considered most important for spermatogenesis. microdeletions of these regions are thought to be involved in some cases of azoospermic or oligospermic...

2016
Raheleh Masoudi Liusa Mazaheri-Asadi Shahryar Khorasani

Y chromosome microdeletions are the second genetic cause of male infertility. The incidence of Y chromosome microdeletions can vary considerably depending on several factors, including patient selection criteria, population composition, and diagnostic protocols. They are associated with spermatogenic failure and lead to azoospermia or oligozoospermia. The advance in assisted reproductive techno...

Journal: :Turkish journal of urology 2013
Ali Şahin Küçükaslan Vildan Bozok Çetintaş Raşit Altıntaş Aslı Tetik Vardarlı Zeynep Mutlu Murat Ulukuş Bülent Semerci Zuhal Eroğlu

OBJECTIVE The aim of this study was to determine the frequencies of Y chromosome microdeletions in infertile azoospermic and oligozoospermic Turkish men and in healthy control subjects. MATERIAL AND METHODS Sixty-four azoospermic and 51 oligozoospermic patients infertile patients, and 70 healthy men who had a child without the aid of assisted reproductive technologies were included in this st...

Background and Aim: The Y-chromosome azoospermic factor (AZF) regions consist of genes whose specific roles and functions in spermatogenesis and fertility have not been completely clarified. Hence, recognition of the association between AZF microdeletions and male infertility has suggestions for the diagnosis, treatment, and genetic counseling. The main objective of the present study was invest...

Abdorrahman Rasekh Elham Konar Hamid Galehdari Hayat Mombeini Saeid Reza Khatami,

Background The androgen receptor (AR) gene contains a polymorphic trinucleotide repeat that encodes a polyglutamine tract in its N-terminal transactivation domain (NTAD). We aimed to find a correlation between the length of this polymorphic tract and azoospermia or oligozoospermia in infertile men living in Khuzestan, Iran. MaterialsAndMethods In this case-control study during two years till 20...

2015
Raheleh Masoudi

Today, with advances in assisted reproductive techniques, many infertile couples are able to have children. However, there is always risk of passing genetic abnormalities associated with infertility from parents to children. Therefore, detection of microdeletions of Y chromosome in patients with spermatogenesis failure seems very important. The purpose of this study was to determine the frequen...

Journal: :journal of reproduction and infertility 0

background: while multiple factors can contribute to male infertility, genetic factors, such as chromosomal disorders or y-chromosome microdeletion, are responsible for about 10% of male infertility. considering the role of y-chromosome microdeletions in men with oligozoospermia who volunteer for in vitro fertilization (ivf), the prevalence of such microdeletions in each particular community ne...

Journal: :Yeni üroloji dergisi 2021

Objective: Advances in the science of genetics and development assisted reproductive techniques focus on genetic causes infertility. The aim this research is to reveal abnormalities terms sex chromosome aneuploidy Y microdeletions. Material Methods: A total 350 patients with azoospermia or severe oligozoospermia were selected. After general examination laboratory investigations performed, carto...

Journal: :journal of paramedical sciences 0
farhad shaveisi-zadeh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran kimia davarian department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran abolfazl movafagh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran reza mirfakhraie molecular pathology research center, imam reza hospital, kermanshah university of medical sciences, kermanshah, iran zahra rostami-far department of biochemistry, school of medicine, kermanshah university of medical sciences, kermanshah, iran reza alibakhshi department of biochemistry, school of medicine, kermanshah university of medical sciences, kermanshah, iran.

about 15% of couples have infertility problems, half of which are related to male factors. cytogenetic and genetic disorders account for about 10% of the male infertility problems. the aim of this study was to determine the frequency and types of both cytogenetic abnormalities and azf microdeletions of y chromosome in idiopathic azoospermic and oligospermic infertile men in west of iran. in thi...

Journal: :Urology journal 2006
Hossein Sadeghi-Nejad Farhat Farrokhi

INTRODUCTION We reviewed the most recent advances in the genetics of male infertility focusing on Y chromosome microdeletions. MATERIALS AND METHODS We searched the literature using the PubMed and skimmed articles published from January 1998 to October 2007. The keywords were the Y chromosome, microdeletions, male infertility, and azoospermia factor (AZF). The full texts of the relevant artic...

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