نتایج جستجو برای: heart defects

تعداد نتایج: 507205  

ژورنال: طب کار 2017

Introduction: Recognition of maternal exposure to solvents and its relationship with congenital heart defects in infants can be effective in identifying effective environmental factors in the occurrence of anomalies. The aim of this study was to determine the relationship between maternal occupational exposure to solvent and birth congenital heart defects in infants. Method: In this case contr...

Journal: :the journal of tehran university heart center 0
hamzullah khan department of cardiology, postgraduate medical institute, lady reading hospital, peshawar, pakistan. hikmatullah jan department of cardiology, postgraduate medical institute, lady reading hospital, peshawar, pakistan. muhammad hafizullah department of cardiology, postgraduate medical institute, lady reading hospital, peshawar, pakistan.

background: we sought to determine the frequency of the risk factors for congestive cardiac failure (ccf) in a tertiary care hospital in peshawar, pakistan. methods: this retrospective, observational study was conducted in the department of cardiology, postgraduate medical institute, lady reading hospital peshawar, from march 2005 to september 2007. relevant information regarding the risk facto...

Journal: :Circulation. Cardiovascular genetics 2013
Nicole Corsten-Janssen Wilhelmina S Kerstjens-Frederikse Gideon J du Marchie Sarvaas Maria E Baardman Marian K Bakker Jorieke E H Bergman Hanne D Hove Ketil R Heimdal Cecilie F Rustad Raoul C M Hennekam Robert M W Hofstra Lies H Hoefsloot Conny M A Van Ravenswaaij-Arts Livia Kapusta

BACKGROUND Loss-of-function mutations in CHD7 cause Coloboma, Heart Disease, Atresia of Choanae, Retardation of Growth and/or Development, Genital Hypoplasia, and Ear Abnormalities With or Without Deafness (CHARGE) syndrome, a variable combination of multiple congenital malformations including heart defects. Heart defects are reported in 70% to 92% of patients with a CHD7 mutation, but most stu...

Journal: :the journal of tehran university heart center 0
akbar shahmohammadi shaheed rajaie cardiovascular medical and research center, tehran, iran. nader givtaj shaheed rajaie cardiovascular medical and research center, tehran, iran. seyed mohammad dalili shaheed rajaie cardiovascular medical and research center, tehran, iran. rahman ghaffari shaheed rajaie cardiovascular medical and research center, tehran, iran.

congenital left ventricular diverticulum is a rare cardiac malformation. two categories of congenital ventricular diverticulum have been identified with regard to their localization: apical and non-apical. apical diverticula are always associated with midline thoraco-abdominal defects and other heart malformations. non-apical diverticula are always isolated defects. diagnosis is established by ...

Journal: :Pediatric Neurology Briefs 1990

Journal: :Deutsches Aerzteblatt Online 2011

Journal: :American Journal of Preventive Medicine 2015

Journal: :JAMA 2015
Nathalie Auger William D Fraser Jessica Healy-Profitós Laura Arbour

IMPORTANCE The risk of congenital heart defects in infants of women who had preeclampsia during pregnancy is poorly understood, despite shared angiogenic pathways in both conditions. OBJECTIVE To determine the prevalence of congenital heart defects in offspring of women with preeclampsia. DESIGN, SETTING, AND PARTICIPANTS Population-level analysis of live births before discharge, 1989-2012,...

اسلامی موید, ماریه, اسلامی موید, مرضیه, صالحی, فرود, طبسی‌زاده, حامد,

Background: Cerebral arteriovenous malformations are rare congenital anomalies presenting as different symptoms depending on their size and the age of patient. Congestive heart failure is a rare condition in neonatal period and is most common due to structural heart defects, but rarely may be a result of peripheral shunts such as cerebral arteriovenous malformation. Case presentation: A term...

Fereshteh Rezakhanlu, Pupak Derakhshandeh-Peykar, Reza Ebrahimzadeh-Vesal, Seyed kianush Hosseini,

Holt-Oram syndrome (HOS) is a developmental disorder inherited in an autosomal-dominant pattern. Affected organs are the heart and forelimbs with upper extremity skeletal defects and congenital heart malformation. In this study we present three cases of HOS in the same family. In one of these three individuals we detected a transition of C to T (CTG-GTT, V205V) in exon 7 of the TBX5 gene. This ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید