نتایج جستجو برای: chromosomal abnormality

تعداد نتایج: 189386  

Journal: :acta medica iranica 0
m. t. akbari. f. behjati. ashtiani m. khaleghian

this report presents the cytogenetic findings (g -banded chromosomal analysis} in 383 cases referred for suspected chromosomal abnormalities because of abnormal clinical features. chromosomal aberrations were found in 63 116.5%) of these cases, free trisomy 21 (7%) being the most common abnormality , followed by 47, xxykaryotype (4%). the breakdown figures for each group is discussed in the text.

Journal: :genetics in the 3rd millennium 0
فرحناز ریحانی فر farahnaz reyhanifar behbood hospital, tabriz university of medical sciences, tabriz, iranبیمارستان تخصصی بهبود، دانشگاه علوم پزشکی تبریز، تبریز، ایران نادر لطفعلی زاده nader lotfalizadeh behbood hospital, tabriz university of medical sciences, tabriz, iranبیمارستان تخصصی بهبود، دانشگاه علوم پزشکی تبریز، تبریز، ایران نوشین سرخکوه آذری noshin sorkhkooheazari behbood hospital, tabriz university of medical sciences, tabriz, iranبیمارستان تخصصی بهبود، دانشگاه علوم پزشکی تبریز، تبریز، ایران اسدالله قنبری asadolah ganbari behbood hospital, tabriz university of medical sciences, tabriz, iranبیمارستان تخصصی بهبود، دانشگاه علوم پزشکی تبریز، تبریز، ایران سعید شبستری saeed shabestari behbood hospital, tabriz university of medical sciences, tabriz, iranبیمارستان تخصصی بهبود، دانشگاه علوم پزشکی تبریز، تبریز، ایران پور بنیادی poorbonyadi behbood hospital, tabriz university of medical sciences, tabriz, iranبیمارستان تخصصی بهبود، دانشگاه علوم پزشکی تبریز، تبریز، ایران

amniocentesis is a known and accessible method for prenatal diagnosis. it is performed after the 15th week of gestation. in this method, about 20 ml of the amniotic fluid is aspirated and evaluated for biochemical tests, culture of amniocytes for karyotype, dna analysis and linkage tests based on indication. the objective of this study was to determine the indications, results and complications...

2005
S. Amudha N. Aruna S. Rajangam

BACKGROUND: Consanguinity is defined as the marriage between close relatives. The deleterious effects associated with consanguinity may be caused by the expression of rare recessive genes inherited from common ancestors. AIMS AND OBJECTIVES: The present study was undertaken to analyze the effect of consanguinity on chromosomal abnormality (CA). METHODS AND MATERIALS: During last 6 years period,...

Journal: :international journal of fertility and sterility 0

0

Journal: :INTERNATIONAL JOURNAL OF HUMAN GENETICS 2015

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...

Journal: :journal of biotechnology and health sciences 0
reza najafipour cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran javad ansari cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran manijeh jalilvand cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran sahar moghbelinejad cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran; cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran. tel: +98-2813336001, fax: +98-2813324970

background chromosomal abnormality plays an important role in different types of miscarriages. objectives the present study was designed to investigation chromosomal anomalies in three groups of couples with recurrent abortion (ra), spontaneous abortion (sa) and still birth (sb). patients and methods in this retrospective study, the frequency of chromosomal aberrations was investigated among 26...

2016
Sayee Rajangam Preetha Tilak Sonia Dhawan

Chromosomal abnormality is one of the causal factors in the formation of the congenital heart defects. 65 patients (33 male and 32 female) with heart defects were referred for karyotyping and counseling. Chromosomal abnormalities were detected in 27 (41.5%) and 38 had a normal karyotype. Numerical abnormality was found in 21 (77.8%) and structural in 6 (22.2%), numerical was detected in 14 fema...

Journal: :International Journal of Health Sciences (IJHS) 2022

Background and Objectives: studying chromosomal changes for anemia patients of children age (3month-12years ) in the city kut diagnosing those abnormalities resulting from having Methods: The chromosomes Patients to were analyzed studied using cytogenetic analysis detect aberrations caused by after collecting blood samples Al-Karama Teaching Hospital as well clinics Kut.Results: Chromosomal all...

Iran Rashidi, Javad Mohammadi Asl

Objective: Approximately 15-20% of clinically recognizable pregnancies end in spontaneous abortion. The incidence of chromosomal abnormalities in those abortions is as high as 50%.A modest but clinically important proportion of spontaneous abortions is caused by a balanced chromosomal aberration in one o...

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