نتایج جستجو برای: cardiac anomaly

تعداد نتایج: 313453  

2014
Ersin Ozturk Cahit Kafadar Mehmet Dogan Omer Uz

Dear Editor, We read with interest the article of Chou et al. (1). The authors reviewed the multidetector computed tomography (CT) findings of congenital coronary sinus anomalies and reported two cases of coronary sinus anomaly. We would like to share our observations, with respect to coronary sinus anomalies, with our colleagues. For better clinical outcomes, coronary venous variations should ...

2016
Saji Philip Sarasa Bharati Kottureth Mammen Cherian Saroja Bharati

Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination co...

Journal: :caspian journal of pediatrics 0
soheil osia non-communicable pediatric diseases research center abbas hadipour non-communicable pediatric diseases research center mahsa moshrefi babol university of medical sciences mohaddese mirzapour faculty of traditional iranian medicine

background: the most common congenital abnormality of esophagus is esophageal atresia (ea) that can occur with or without tracheoesophageal fistula. other associated anomalies are the leading cause of death in these patients. the present study aimed to evaluate the main complication, outcomes and cause of death in neonate with ea repaired in amirkola children’s hospital (ach), iran within a 13 ...

غفاری , جواد, غفاری ساروی , وجیهه, فریبرزی , محمدرضا,

Cornelia De Lange is a rare congenital syndrome with multiple anomalies including Facial dysmorphism, hirsutism, height, weight and head circumflex retardations, cardiac defects, gastrointestinal and renal defects and extremity anomaly. Prevalence of this syndrome is 1 to 30000 or 1 to 50000. The diagnosis of this syndrome is based on clinical evidence. Genetic foundation is known to have two...

Journal: :archives of cardiovascular imaging 0
hamidreza pouraliakbar assistant professor of radiology, rajaie cardiovascular, medical and research center, tehran, ir iran anita sadeghpour professor of cardiology, fellow of echocardiography, rajaie cardiovascular, medical and research center, tehran, ir iran azin alizadehasl associated professor of cardiology, fellow of echocardiography, rajaie cardiovascular, medical and research center, tehran, ir iran; associated professor of cardiology, fellow of echocardiography, rajaie cardiovascular, medical, and research center, tehran, ir iran. tel: +98-2123922190 ata firoozi interventional cardiologist, associate professor of cardiology, rajaie cardiovascular, medical and research center, tehran, ir iran kianoush homightoun fellow of echocardiography, rajaie cardiovascular, medical and research center, tehran, ir iran nazila alborzi cardiologist, fellow of echocardiography, shafa cardiovascular hospital, gorgan, ir iran

coronary-cameral fistulas (ccfs) constitute a rare anomaly that can be incidentally detected during angiography. ccfs are solitary, large or small assemblies that originate from coronary arteries and enter one of the cardiac chambers. we describe a 29-year-old woman, who referred to our clinic with the chief complaints of palpitation, atypical chest pain, and dyspnea on exertion (functional cla...

Journal: :British heart journal 1974
G Bevilacqua

A rare type of congenital mitral regurgitation is presented for the first time as an isolated cardiac anomaly. The malformation consists of a particular arrangement of the chordae tendineae of the posterior leaflet: the chordae, leaving the free margin or the undersurface, insert into the latter once again. A definition of the anomaly and a classification of all the chordal anomaliesfound in co...

Journal: :International journal of clinical and experimental pathology 2015
Zhongshan Gou Yihua He Ye Zhang Xiaoyan Gu

Double aortic arch (DAA) is the most common congenital anomaly of the aortic arch system, in which the trachea and esophagus are completely encircled by connected segments of the aortic arch and its branches, often resulting in variable airway compression. We present a case of fetal DAA prenatally diagnosed by fetal echocardiography and clearly confirmed at autopsy. The autopsy visualization al...

Journal: :British heart journal 1985
G A Russell P G Stovin

At birth an infant was found to have an unusual series of abnormalities with a coronary sinus type atrial septal defect complicating pulmonary atresia with an intact ventricular septum and Ebstein's anomaly. The functionally important anomalies were diagnosed by echocardiography and cardiac catheterisation. The coronary sinus defect and Ebstein's anomaly were detected only at necropsy. Although...

2011
Woo-Sik Han Pyo Won Park Seong-Ho Cho

Anomalous origin of a coronary aortic artery is a rare cardiac anomaly. Although it can cause angina, syncope, and palpitations, most patients are asymptomatic. This anomaly requires surgical treatment or intervention because it is associated with sudden death. Several surgical techniques, such as coronary reimplantation, coronary artery bypass grafting (CABG), unroofing, and neo-ostium formati...

2016
Tatsuya Fukami Maki Goto Sakiko Matsuoka Sumire Sorano Atsushi Tohyama Hiroko Yamamoto Sumie Nakamura Ryoei Matsuoka Hiroshi Tsujioka Fuyuki Eguchi

Our patient was diagnosed as having discordant twin growth with Ebstein's anomaly in the larger fetus. Cardiac function was deteriorated in accordance with progression of gestational age. Our observation indicated cardiac failure of the larger fetus. The most important issue in this situation is management of the timing of delivery.

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