نتایج جستجو برای: chromosome microdeletion

تعداد نتایج: 120218  

Alizadeh-Nili H Ghoraeian P Moghbelinejad S Mohseni-Meybodi A Mozdarani H, Nazari E Salimi M

Background: Sperm chromatin insufficiencies leading to low sperm count and quality, infertility and transmission of chromosomal microdeletion and aneuploidies to next generations can be due to exposure to environmental pollutions, chemicals and natural or manmade ionizing radiation. In this project which has continued for more than 10 years and is unique in many technical aspects in Iran and in...

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...

2017
Hong‐Dan Wang Lin Liu Dong Wu Tao Li Cun‐Ying Cui Lian‐Zhong Zhang Cheng‐Zeng Wang

BACKGROUND Little information is available regarding the penetrance of 1q21.1 copy number variants (CNVs). In the present study, we explored the clinical significance of 1q21.1 microdeletion or microduplication. METHODS In four families, chromosome karyotype was analyzed using G-banding karyotype analysis technology. CNVs were detected using array-comparative genomic hybridization (aCGH) and ...

2014
Sathiya Maran Mehboob Alam Pasha Thirumulu Ponnuraj Kannan

Microdeletion syndromes are due to submicroscopic chromosomal deletions and display a complex clinical and behavioral phenotype. This occurs because of an imbalance of normal dosage of genes that are present in that segment of chromosome. Many clinical characteristics of the well-known microdeletion syndromes are very specific and have been well defined. It is not always possible to detect thes...

2014
Adrian Mc Cormack Juliet Taylor Leah Te Weehi Donald R Love Alice M George

Concurrent cryptic microdeletion and microduplication syndromes have recently started to reveal themselves with the advent of microarray technology. Analysis has shown that low-copy repeats (LCRs) have allowed chromosome regions throughout the genome to become hotspots for nonallelic homologous recombination to take place. Here, we report a case of a 7.5-year-old girl who manifests microcephaly...

Journal: :iranian red crescent medical journal 0
s ghorbian department of biology, science and research branch, islamic azad university, iran k saliminejad department of biology, science and research branch, islamic azad university, iran mr sadeghi department of biology, science and research branch, islamic azad university, iran ghr javadi department of biology, science and research branch, islamic azad university, iran k kamali department of biology, science and research branch, islamic azad university, iran n amirjannati department of biology, science and research branch, islamic azad university, iran

2010
Levent Sagnak Hamit Ersoy Ugur Ozok Asir Eraslan Kanay Yararbas Goksel Goktug Ajlan Tukun

INTRODUCTION The aim of study is determining the cost-effectiveness of detection analysis in the presence of exceptional patients who have mild semen disorders, and beware of unnecessary varicocele repairs; and to ascertain whether patients with clinical varicocele should undergo Y chromosome (Yq) microdeletion analysis as a routine procedure. MATERIAL AND METHODS Varicocele with reflux was d...

Journal: :European journal of medical genetics 2011
Christèle Dubourg Damien Sanlaville Martine Doco-Fenzy Cédric Le Caignec Chantal Missirian Sylvie Jaillard Caroline Schluth-Bolard Emilie Landais Odile Boute Nicole Philip Annick Toutain Albert David Patrick Edery Anne Moncla Dominique Martin-Coignard Catherine Vincent-Delorme Isabelle Mortemousque Bénédicte Duban-Bedu Sèverine Drunat Mylène Beri Jean Mosser Sylvie Odent Véronique David Joris Andrieux

Chromosome 17q21.31 microdeletion was one of the first genomic disorders identified by chromosome microarrays. We report here the clinical and molecular characterization of a new series of 14 French patients with this microdeletion syndrome. The most frequent clinical features were hypotonia, developmental delay and facial dysmorphism, but scaphocephaly, prenatal ischemic infarction and percept...

2015
Ines Quintela Montse Fernandez-Prieto Lorena Gomez-Guerrero Mariela Resches Jesus Eiris Francisco Barros Angel Carracedo

We report on a male patient with severe autistic disorder, lack of oral language, and dysmorphic features who carries a rare interstitial microdeletion of 4.96 Mb at chromosome 6q14.1-q15. The patient also harbors a maternally inherited copy number gain of 1.69 Mb at chromosome Xp22.31, whose pathogenicity is under debate.

Journal: :Missouri dental journal 1984
R T Couper J J Couper

Prader-Willi syndrome is a multi system disorder characterized by neonatal hypotonia, later obesity, hyperphagia and mental retardation. It occurs sporadically, either as a result of microdeletion of chromosome 15p (70%) or as a result of maternal disomy of chromosome 15 (30%). The major problems encountered by parents are those of hyperphagia, food-seeking and obesity, and conduct disorder, pa...

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