نتایج جستجو برای: congenital • heart septal defect

تعداد نتایج: 578664  

Journal: :the journal of tehran university heart center 0
bagher nikyar gorgan congenital malformations research center, golestan university of medical sciences, gorgan, iran. maliheh sedehi gorgan congenital malformations research center, golestan university of medical sciences, gorgan, iran. mostafa qorbani department of public health, alborz university of medical sciences, karaj, iran and non-communicable diseases research center, endocrinology and metabolism research insti- tute, tehran university of medical sciences, tehran, iran. arash nikyar cranfield university, london, england. mohammadjafar golalipour gorgan congenital malformations research center, golestan university of medical sciences, gorgan, iran.

background: congenital heart disease (chd) is the most common congenital anomaly in newborns. this study was performed to determine the live birth incidence of chd by ethnicity and sex in gorgan, northern iran. methods: in this longitudinal, hospital-based study, 18162 live births in dezyani hospital in gorgan, north of iran, were screened for chd, from 2007 through 2009. clinical examination, ...

Journal: :the journal of tehran university heart center 0
ramin baghaei tehrani rajaee heart center, iran university of medical sciences, tehran, iran. alireza rostami rajaee heart center, iran university of medical sciences, tehran, iran. hosein ali basiri rajaee heart center, iran university of medical sciences, tehran, iran. hojatollah mortezaiian rajaee heart center, iran university of medical sciences, tehran, iran.

this is a case presentation of a 26-year-old woman with a moderate-sized atrial septal secundum defect (17mm) who underwent catheterism, during which an amplatzer septal occluder number 26 was inserted successfully. on the second postoperative day, she deteriorated and a clinical examination showed a typical tamponade. after a percutaneous aspiration of the pericardial cavity and transient impr...

ژورنال: یافته 2014
احمدی پور, شکوفه , بهاروند, بابک , محسن زاده, اعظم , ساکت, ساسان ,

Background: Congenital heart disease is the most common congenital malformations in newborns. The aim of this study was to determine the prevalence and types of congenital heart disease in babies born in the city of Khorramabad. Materials and Methods: The present study was a descriptive cross-sectional. Sampling method was census. All babies born in the city of Khorramabad from 2007 to 2011, w...

Journal: :the journal of tehran university heart center 0
maryam esmaeilzadeh shaheed rajaei cardiovascular medical and research center, tehran, iran. azadeh sadatnaseri sina general hospital, tehran university of medical sciences, tehran, iran. feridoun noohi shaheed rajaei cardiovascular medical and research center, tehran, iran. majid maleki shaheed rajaei cardiovascular medical and research center, tehran, iran. anita sadeghpour shaheed rajaei cardiovascular medical and research center, tehran, iran. ahmad mohebbi shaheed rajaei cardiovascular medical and research center, tehran, iran.

background: there is some evidence indicating improvement in myocardial performance after atrial septal defect closure, either device closure or surgical, but ventricular dyssynchrony has not been evaluated before and after surgical closure. the aim of this study was to evaluate ventricular mechanical dyssynchrony in patients with atrial septal defect before and after surgical closure. methods:...

Journal: :the journal of tehran university heart center 0
rachid el haouati cardiovascular surgery unit, mohamed vi universitary hospital, marrakech, morocco. yassine boukaidi cardiovascular surgery unit, mohamed vi universitary hospital, marrakech, morocco. zahira zouizra cardiovascular surgery unit, mohamed vi universitary hospital, marrakech, morocco. drissi boumzebra cardiovascular surgery unit, mohamed vi universitary hospital, marrakech, morocco.

aortopulmonary window (apw) is a rare congenital malformation. it results from an incomplete division between the ascending aorta and the pulmonary artery. we describe a 26-year-old male, who presented with a grade ii exertional dyspnea and palpitations. echocardiography revealed an apw with an ascending aorta aneurysm. he underwent surgery under cardiopulmonary bypass without aortic cross-clam...

M.H Torabi-Nezhad M.M Bagheri M.R Baneshi Z Jamali

Background & aim: Congenital heart disease is one of the most common malformations at birth that require timely recognition and treatment. The aim of this study was to determine the prevalence and etiology of detected heart murmurs and association between congenital heart disease and heart murmurs. Recognition of murmurs etiology would help us to manage and treat them properly. Methods: In this...

Journal: :archives of cardiovascular imaging 0
sedat altay department of radiology, ataturk research and education hospital, katip celebi university, izmir, turkey; department of radiology, ataturk research and education hospital, katip celebi university, izmir, turkey. tel: +90-5332435440, fax: +90-2322431530 canan altay department of radiology, faculty of medicine, dokuz eylul university, izmir, turkey nezahat erdogan department of radiology, ataturk research and education hospital, katip celebi university, izmir, turkey sebnem karasu department of radiology, ataturk research and education hospital, katip celebi university, izmir, turkey orhan oyar department of radiology, ataturk research and education hospital, katip celebi university, izmir, turkey

the most frequent congenital heart defects in the neonatal period are ventricular septal defects. ventricular septal aneurysms can rarely develop from an interventricular septal (ivs) defect in adults. we describe a 47-year-old man with an aneurysm in the ivs growing towards the right ventricle, which was confirmed by cardiac computed tomographic angiography and was missed by echocardiography.

Partial muscular inter-ventricular septal defect (VSD) or Pacman heart is a rare congenital or occasionally acquired anomaly. Concurrent Pacman heart and Shone's complex are extremely rare and have never been reported until now. We described a 37-year-old male patient with congenital Pacman heart, flail mitral valve (FMV), and a history of multiple congenital anomalies, including subvalvular ao...

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: :archives of cardiovascular imaging 0
anita sadeghpour echocardiography research center, rajaie cardiovascular medical and research center, iran university medical science, tehran, ir iran; md, fase, facc, echocardiography research center, rajaie cardiovascular medical and research center, tehran, ir iran. tel: +98-2123922145, fax: +98-2122042026 majid kyavar rajaie cardiovascular medical and research center, iran university medical science, tehran, ir iran mohammad ali yousefnia rajaie cardiovascular medical and research center, iran university medical science, tehran, ir iran soheila chamanian mashhad university medical sciences, mashhad, ir iran zahra khajali rajaie cardiovascular medical and research center, iran university medical science, tehran, ir iran zahra alizadeh sani rajaie cardiovascular medical and research center, iran university medical science, tehran, ir iran

abstract hypoplastic right ventricular is a rare congenital heart disease. a few cases have been reported. we presented a case with hypoplastic right ventricular and multiple associated anomaly (ventricular septal defect, atrial septal defect and pulmonary stenosis) in whom the main concern was whether biventricular repair or fontan type surgery would be the optimal management in this patient. ...

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