chromosomal anomalies in infertile azoospermic and oligospermic men

نویسندگان

پریسا کلانتری

kalantari p حوری سپهری

sepehri h محمدتقی اکبری

akbari mt زهرا اوسطی آشتیانی

osati ashtiani z فرخنده بهجتی

چکیده

in this study, chromosome analyses were performed on 70 infertile azoospermic and oligospermic (<20 million/ml) men, and also cultures of peripheral blood lymphocytes by high resolution banding method were analysed as well. it is revealed 8 (11.43 percent) men with chromosomal abnormality. there were 31.4 percent patients with azoospermia and 68.6 percent with oligospermia from several thousands to 20×10^6 million/ml and their duration of infertility was at least 2 years. all patients with numerical chromosome anomalies had azoospermia and the most frequent anomaly was 47, xxy chromosomal constitution (klinfelter&apos;s syndrome), found in 8.57 percent of patients. we found that chromosomal anomalies found in this study were sex chromosome anomalies and an increased rate of numerical chromosomal abnormalities was among men with azoospermia. as a conclusion, we suggest that all men with azoospermia be considered for cytogenetical evaluation.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Frequency of Y Chromosome Microdeletions in Azoospermic and Oligospermic Iranian Infertile Men

Background and Aims: Azoospermia factor (AZF) region of the Y-chromosome has several genes which are responsible for normal spermatogenesis. Microdeletions of these genes are associated with azoospermia and oligospermia. These microdeletions are too small to be detected by karyotyping. They can be easily identified using polymerase chain reaction. The aim of this study is to determine the frequ...

متن کامل

The frequency of Yq microdeletion in azoospermic and oligospermic Iranian infertile men

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 ...

متن کامل

Chromosomal Aneuploidy in Azoospermic Men

The aim of this study was to estimate the prevalence of chromosome abnormalities in patients with azoospermia, in our material. Preoperative evaluation included routine andrological investigations with 2 semen analysis, ultrasound, hormonal and genetic examinations. In the last three years, 73 biopsies were performed for testicular sperm extraction in 71 patients. Non-obstructive azoospermia wa...

متن کامل

P-208: Analysis of H2BFWT Gene Alterations in Severe Oligospermic and Azoospermic Infertile Men Referred to Royan Institute

Background: Telomeres play a dramatic role in sperm pronuclei formation and subsequently successful fertilization. The H2B family, member W, testis specific (H2BFWT) gene encodes a testis specific histone that colocalized with telomeric sequences and interfere in the dynamic rearrangement of telomeres at late stages of spermatogenesis. H2BFWT is essential for transmission of the telomeric chrom...

متن کامل

Relationship of serum and seminal plasma zinc levels and serum testosterone in oligospermic and azoospermic infertile men.

OBJECTIVE To measure the zinc level in fertile and infertile population and to find out relationship of serum and seminal plasma zinc levels and serum testosterone in oligospermic and azoospermic infertile men. DESIGN Comparative study. PLACE AND DURATION OF STUDY The Infertility Clinic, Jinnah Postgraduate Medical Center (JPMC), Karachi, from January 2002-July 2003. PATIENTS AND METHODS ...

متن کامل

P-236: Haplotype Analysis of The H2B.W Gene in Severe Oligospermic and Azoospermic Infertile Men Referred to Royan Institute

Background: Recent studies demonstrated the multifactorial and chronic nature of male infertility, including mutations of some known spermatogenesis-related genes. The H2B family, member W (H2B.W) gene is one of the testis specific histone variant genes that encodes a sperm telomere-binding protein, required for reorganization and integration of sperm chromosomes. The objective of the present s...

متن کامل

منابع من

با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید


عنوان ژورنال:
مجله دانشکده پزشکی دانشگاه علوم پزشکی تهران

جلد ۵۹، شماره ۳، صفحات ۶۰-۷۱

کلمات کلیدی

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023