نتایج جستجو برای: chromosomal abmormalities

تعداد نتایج: 47372  

Journal: :بینا 0
مهرناز نارویی نژاد m narooie-nejad zahedan university of medical sciences, zahedan, iran- مرکز تحقیقات ژنتیک در بیماری های غیرواگیر- دانشگاه علوم پزشکی زاهدان- زاهدان- ایران حبیب اله زنجانی h zanjani zahedan university of medical sciences, zahedan, iranدانشگاه علوم پزشکی زاهدان- زاهدان- ایران رضا اکبرپور r akbarpour zahedan university of medical sciences, zahedan, iranدانشگاه علوم پزشکی فسا- فارس- ایران علی خواجه a khaje zahedan university of medical sciences, zahedan, iranمرکز تحقیقات سلامت کودکان و نوجوانان- دانشگاه علوم پزشکی زاهدان- زاهدان- ایران

purpose: to assess the frequency and type of associated malformations and chromosomal anomalies among patients with anophthalmia, microphthalmia, and coloboma in sistan and baluchestan province. methods: patients with a clinical diagnosis of anophthalmia, microphthalmia, or coloboma were examined to find any anomaly in craniofacial, muscle-skeletal, cardiac, neurologic and urogenital systems. a...

Journal: :iranian journal of radiation research 0
d. fatehi department of medical physics, faculty of medicine, shahrekord university of medical sciences, shahrekord, iran h. mozdarani department of medical genetics, faculty of medical sciences, tarbiat modares university,tehran, iran

background: to evaluate the effects of hyperthermia (ht) on the frequency of chromosomal aberrations induced by a low dose of neutron or γ-rays in human peripheral blood lymphocytes. materials and methods: blood samples were exposed to ht (41.5°c for 30 and 60min, 43°c for 15 and 30min), 10 cgy neutron or γ-rays, ht + neutron/γ, and neutron/γ + ht. after standard cell culture, harvesting, fixat...

Journal: :archives of medical laboratory sciences 0
zahra meshkat professor; department of virology, tarbiat modares university, tehran nayere khadem ghaebi mohammad khajedaluee zahra aghili sina rostami

background: recurrent miscarriage is defined as two or more recurrent spontaneous miscarriages. several causes have been suggested, among which, chromosomal abnormalities in couples is considered to have a role in this regard. however, its significance varies among different populations. the present study was carried out to evaluate the prevalence of chromosomal aberrations in couples with recu...

حوری سپهری, , زهرا اوسطی آشتیانی, , فرخنده بهجتی, , محمدتقی اکبری, , پریسا کلانتری, ,

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 thousand...

Ring chromosomes are rare chromosomal disorders that usually appear to occur de novo. A ring chromosome forms when due to deletion both ends of chromosome fuse with each other. Depending on the amount of chromosomal deletion, the clinical manifestations may be different. So, ring 18 syndrome is characterized by severe mental growth retardation as well as microcephaly, brain and ocular malformat...

Aghamohammadian J Hassanzadeh-Nazarabadi M, Kerachian MA Mojarrad M Shekouhi S Tabari A

Background: Spontaneous abortion (SAb) is the most common complication of early pregnancy. Numerous risk factors are associated with an increased risk of pregnancy loss such as: Maternally age, previous spontaneous abortion, prolonged ovulation to implantation, Gravidity, Interval Prolonged time to pregnancy, Balanced chromosomal translocations and Genetic disorders. The aim of this study was t...

D. H. Gonzales, Gh. Azizian, H. Samavat, M. R. D. Seaward,

Background: Most of our current understanding of the biological effects of exposure to ionising radiation is based on conventional cytogenetic techniques, which enable us to determine the relationship between chromosomal aberration and dose received by radiation workers. However, conventional techniques have numerous limitations and chromosomal aberrations can be easily missed. Since FISH plays...

Journal: :iranian journal of basic medical sciences 0
sahar moghbeli nejad department of medical genetics, school of medical sciences, tarbiat modares university, tehran, iran national cell bank of iran, pasteur institute, tehran, iran. hossein mozdarani department of medical genetics, school of medical sciences, tarbiat modares university, tehran, iran mohammad ali shokrghozar national cell bank of iran, pasteur institute, tehran, iran. vahideh farahat national cell bank of iran, pasteur institute, tehran, iran.

objective(s) the main objective of this study was to investigate the status of chromosome stability in 3 human-mouse hybridoma cell lines over a period of time in various passages. materials and methods metaphase spreads from 3 human-mouse cell lines (hf2x653, spmo-4 and f3b6) that had been cultured in 4 successive passages, from 1 to 4 weeks, were prepared and analyzed. metaphase chromosomes s...

Journal: :iranian journal of neurology 0
abbas tafakhori department of neurology, school of medicine, imam khomeini hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran. vajiheh aghamollaii department of neurology, school of medicine, roozbeh hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran. sara faghihi-kashani department of neurology, school of medicine, tehran university of medical sciences, tehran, iran. payam sarraf department of neurology, school of medicine, imam khomeini hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran. laleh habibi department of medical genetics, school of medicine, tehran university of medical sciences, tehran, iran.

epilepsy is one of the most common neurological disorders. studies have demonstrated that genetic factors have a strong role in etiology of epilepsy. mutations in genes encoding ion channels, neurotransmitters and other proteins involved in the neuronal biology have been recognized in different types of this disease. moreover, some chromosomal aberration including ring chromosomes will result i...

Journal: :iranian journal of public health 0
a tahmasebpour n baradaran rafiee s ghaffari a jamal

background: to study the outcome of cases with nuchal translucency (nt) ≥ 95th centile in the first trimester of pregnancy. methods: this cross sectional study was performed at iranian fetal medicine foundation (fmf) between january 2009 and december 2011. totally, 186 cases with nt≥ 95th centile who attended for the first trimester screening were studied. all cases with increased nt including ...

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