نتایج جستجو برای: microdeletions

تعداد نتایج: 900  

2017
Prafulla S. Ambulkar Sunil S. Pande

Genetic factors cause about 15% of male infertility and microdeletions of Y chromosome is one of the genetic causes in idiopathic infertile men. Azoospermia factors (AZFa, AZFb, and AZFc) on Yq long arm are most important for spermatogenesis. For analysis of microdeletions in the AZF regions by sequence-tagged-site (STS) PCR is important screening method for infertility. An attempt has been mad...

2018
Afsaneh Mojtabanezhad Shariatpanahi Hassan Ahmadnia Adam Torkamanzehi Mahnaz Mansouri Torshizi Mohammad Amin Kerachian

Background Approximately 15% of couples are infertile with the male factor explaining approximately 50% of the cases. One of the main genetic factors playing a role in male infertility is Y chromosomal microdeletions within the proximal long arm of the Y chromosome (Yq11), named the azoospermia factor (AZF) region. Recent studies have shown there is a potential connection between deletions of t...

Journal: :Asian journal of andrology 2006
Anurag Mitra Rima Dada Rajeev Kumar Narmada Prasad Gupta Kiran Kucheria Satish Kumar Gupta

AIM To study the occurrence of Y chromosome microdeletions in azoospermic patients with Klinefelter's syndrome (KFS). METHODS Blood and semen samples were collected from azoospermic patients with KFS (n = 14) and a control group of men of proven fertility (n = 13). Semen analysis was done according to World Health Organization (WHO) guidelines. Blood samples were processed for karyotyping, fl...

Journal: :American journal of medical genetics. Part A 2003
Cláudia M B Carvalho Masato Fujisawa Toshiro Shirakawa Akinobu Gotoh Sadao Kamidono Tatiana Freitas Paulo Sidney E B Santos Juliane Rocha Sérgio D J Pena Fabrício R Santos

The Y chromosome carries several genes involved in spermatogenesis, which are distributed in three regions in the euchromatic part of the long arm, called AZFa (azoospermia factor a), AZFb, and AZFc. Microdeletions in these regions have been seen in 10-15% of sterile males with azoospermia or severe oligozoospermia. The relatively high de novo occurrence of these microdeletion events might be d...

2013
Mohammad Ali Zaimy Seyyed Mehdi Kalantar Mohammad Hasan Sheikhha Tahere Jahaninejad Hossein Pashaiefar Jalal Ghasemzadeh Mahnaz Zahraei

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 ...

Journal: :Journal of medical genetics 2005
K Tatton-Brown J Douglas K Coleman G Baujat K Chandler A Clarke A Collins S Davies F Faravelli H Firth C Garrett H Hughes B Kerr J Liebelt W Reardon G B Schaefer M Splitt I K Temple D Waggoner D D Weaver L Wilson T Cole V Cormier-Daire A Irrthum N Rahman

BACKGROUND Sotos syndrome is characterised by learning difficulties, overgrowth, and a typical facial appearance. Microdeletions at 5q35.3, encompassing NSD1, are responsible for approximately 10% of non-Japanese cases of Sotos. In contrast, a recurrent approximately 2 Mb microdeletion has been reported as responsible for approximately 50% of Japanese cases of Sotos. METHODS We screened 471 c...

2013
Rubina Tabassum Siddiqui Nosheen Mujtaba Mamoona Naz

BACKGROUND Microdeletions of the azoospermia factor locus of the long arm of Y chromosome are an etiological factor of severe oligozoospermia or azoospermia. OBJECTIVE The aim of this study was to investigate the prevalence of Y-chromosome microdeletions in AZF region and their role in infertility in Pakistani population. MATERIALS AND METHODS The type of deletions in AZF locus were detecte...

Journal: :modares journal of medical sciences: pathobiology 2007
sara pouranvari mehrdad noruzinia aliakbar zinalou saeedreza ghafari masoud houshmand

objective: 22q11.2 chromosomal region is a hot spot for many cytogenetic rearrangements especially microdeletions which are responsible for digeorge and velocardiofacial syndromes. the most characteristic sign in these patients is congenital cardiac conotruncal anomalies. the gold standard diagnostic test for these microdeletions is fish (fluorescent in situ hybridization). however this diagnos...

Journal: :Molecular Syndromology 2021

Mowat-Wilson syndrome (MWS) is a rare autosomal dominant characterized by dysmorphic features, mental retardation, and congenital heart disease (CHD). MWS results from microdeletions of chromosome 2q23 or de novo SNVs involving the <i>ZEB2</i> gene. Here, we report on an Egyptian patient diagnosed chromosomal microarray (CMA). A 1-year-old male child was referred to CHD clinic, Nati...

Journal: :The Indian journal of medical research 2008
Anurag Mitra Rima Dada Rajeev Kumar N P Gupta Kiran Kucheria S K Gupta

BACKGROUND & OBJECTIVE Analysis of the microdeletions in the azoospermia factor (AZF) region of Y chromosome by PCR is an important screening tool in the work-up of infertile males opting for assisted reproductive techniques. In the present study, the Y chromosome microdeletions were analyzed by PCR using primers corresponding to 16 sequence tagged sites (STS) and three genes of the AZF region ...

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