نتایج جستجو برای: chromosomal anomaly

تعداد نتایج: 85966  

ژورنال: حقوق پزشکی 2017
احسانی, معصومه, صالحی مازندرانی, محمد,

Syndrome means a set of physical and mental symptoms which is manifestation of a disease or hereditary anomaly and its Persian equivalent is “Neshanegan”. The cause of this phenomenon is a type of disorder in chromosomal arrangement which happens in the embryonic stages and at the time of cell division. Those who suffer Down syndrome include 47 chromosomes instead of 46 chromosomes ...

Journal: :acta medica iranica 0
sedighah akhavan karbasi department of pediatric, shaheed sadoughi hospital, school of medicine, shaheed sadoughi university of medical sciences, yazd, iran. motaharah golestan department of pediatric, shaheed sadoughi hospital, school of medicine, shaheed sadoughi university of medical sciences, yazd, iran. raziah fallah department of pediatric, shaheed sadoughi hospital, school of medicine, shaheed sadoughi university of medical sciences, yazd, iran. fahimehsadat mirnaseri department of pediatric, shaheed sadoughi hospital, school of medicine, shaheed sadoughi university of medical sciences, yazd, iran. kazem barkhordari department of pediatric, shaheed sadoughi hospital, school of medicine, shaheed sadoughi university of medical sciences, yazd, iran. mahdokht sadr bafghee department of pediatric, shaheed sadoughi hospital, school of medicine, shaheed sadoughi university of medical sciences, yazd, iran.

congenital malformation (cm) will begin to emerge as one of the major childhood health problems .treatment and rehabilitation of children with congenital malformations are costly and complete recovery is usually impossible. the aim of this study was to determine frequency of cm in yazd central city of the islamic republic of iran to find out if there has been any difference in the rate and type...

امیری , مهرانگیز, شبستانی منفرد , علی, هاشم اوغلی , سیدابوالفضل,

Background and purpose : Ït is clearly shown that ionising radiations induce various kinds of DNÂ damages majority of which as sub-lethal damages, are repaired but still some of them are left urepaired and lead to chromosomal aberrations. These chromosomal aberrations in radiation workers, who are occupationally exposed to radiation,could be assayed with cytogenetic evaluation methods.These c...

ژورنال: مجله طب نظامی 2019

Chromosomal abnormalities are able to produce genetic instability, which is the main cause of many diseases. Cytogenetics is analysis of any kind of chromosomal abnormalities. Chromosomal alterations can be divided into structural and numerical abnormalities, both of which play a significant role in the development of many diseases, particularly cancer. Today, most cytogenetic analyzes are perf...

Hans-Christoph Duba Manuela Puchner Maria Maurer, Omar Shebl Peter Oppelt Richard Bernhard Mayer Thomas Ebner

Background Selecting the best embryo for transfer, with the highest chance of achieving a vital pregnancy, is a major goal in current in vitro fertilization (IVF) technology. The high rate of embryonic developmental arrest during IVF treatment is one of the limitations in achieving this goal. Chromosomal abnormalities are possibly linked with chromosomal arrest and selection against abnormal fe...

2013
K. KANAKARAJ MARIAM SURESH

Gastroschisis is a congenital anomaly which shows extra abdominal herniation of fetal bowel loops, occasionally with portions of liver/ stomach, into the amniotic cavity through a paraumbilical defect in the anterior abdominal wall. The defect is usually right sided. Gastroschisis is decreasing in incidence owing to early detection by the advanced techniques in imaging and more efficient and th...

2013
Shin Yun Byun Ryoung Kyoung Lim Kyung Hee Park Yong Hoon Cho Hae Young Kim

PURPOSE Anorectal malformations are often associated with other anomalies, reporting frequency with 40-70%. Gastrointestinal anomalies have been known to be relatively less common than associated anomalies of other organ system. This study was performed to assess a distinctive feature of cases associated with esophageal atresia. METHODS Clinical data (from January 2000 through December 2011) ...

2015
Rahime Nida Ergin Murat Yayla

Objective: The purpose of this study is to show distribution of risk in pregnancies which underwent first trimester combined tests, and investigate general demographic and clinical characteristics of patients, underwent invasive diagnostic tests after screening tests. Methods: Combined test data of first trimester screening in 20082011 were evaluated retrospectively and cross-sectional. After t...

Journal: :Human reproduction update 2009
P O D Pharoah Y Dundar

BACKGROUND The majority of cases of cerebral palsy (CP) have their pathogenesis during fetal development and are a form of congenital anomaly, the aetiology of which is uncertain. Anomalous development of other organs evident at birth is also a congenital anomaly. A small proportion of these are known to be caused by chromosomal or gene abnormalities, environmental teratogens and dietary defici...

Journal: :Blood 1993
M J Kroef W E Fibbe R Mout R P Jansen H L Haak J W Wessels H Van Kamp R Willemze J E Landegent

Interstitial deletions of the long arm of chromosome 5 are among the most characteristic abnormalities observed in myeloid disorders. To assess the lineage involvement of peripheral blood cells from patients with a 5q--anomaly, purified neutrophils, monocytes, T lymphocytes, and B lymphocytes were analyzed for loss of heterozygosity using six different highly polymorphic mininucleotide and dinu...

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