نتایج جستجو برای: cardiac anomalies

تعداد نتایج: 319364  

2016
Youngjin Cho

Symptomatic supraventricular tachycardia is a common indication for radiofrequency catheter ablation treatment. Often, supraventricular tachycardia is associated with sick sinus syndrome, which requires the implantation of a permanent pacemaker. Underlying structural heart diseases such as complex congenital anomalies or a history of prior cardiac surgery can hinder successful procedural treatm...

Journal: :American journal of medical genetics. Part A 2014
Joan K Morris Ester Garne Diana Wellesley Marie-Claude Addor Larraitz Arriola Ingeborg Barisic Judit Beres Fabrizio Bianchi Judith Budd Carlos Matias Dias Miriam Gatt Kari Klungsoyr Babak Khoshnood Anna Latos-Bielenska Carmel Mullaney Vera Nelen Amanda J Neville Mary O'Mahony Annette Queisser-Luft Hanitra Randrianaivo Judith Rankin Anke Rissmann Cath Rounding Antonin Sipek Sylvia Stoianova David Tucker Hermien de Walle Lyubov Yevtushok Maria Loane Helen Dolk

Previous studies have shown that over 40% of babies with Down syndrome have a major cardiac anomaly and are more likely to have other major congenital anomalies. Since 2000, many countries in Europe have introduced national antenatal screening programs for Down syndrome. This study aimed to determine if the introduction of these screening programs and the subsequent termination of prenatally de...

Background & Aims: Congenital anomaly is characterized by any anatomical defects present in a baby at birth that may cause major medical, surgical, or cosmetic consequences. the present study aimed to determine the prevalence of congenital anomalies and related factors among infants in Hamadan Fatemiyeh and Behesht hospitals in 2015.   Materials & Methods: this case series study...

A KHALEGHNEJAD TABARI, D FRANK, HR NOBLETT,

From October 1977 to December 1988, 108 neonates born with esophageal atresia (EA) and/or a tracheoesophageal fistula (TEF) were treated at the Bristol Royal Hospital for Sick Children. An incidence of I :4000-4500 live births was noted. 1I2.4% had the common- type anomaly, 5.5% had pure esophageal atresia, and 6.5% had an H-type anomaly. 2.8% had upper and lower fistulae and 2.8% had uppe...

Journal: :Heart 2011
Wilhelmina S Kerstjens-Frederikse Gideon J Du Marchie Sarvaas Jolien S Ruiter Peter C Van Den Akker Arno M Temmerman Joost P Van Melle Robert M W Hofstra Rolf M F Berger

OBJECTIVES To determine whether offering cardiac screening to relatives of patients with left ventricular outflow tract obstructions (LVOTOs) would be justified. BACKGROUND LVOTOs have been recognised as a group of congenital heart diseases with 'high heritability'. One of the LVOTOs, the bicuspid aortic valve, is often asymptomatic, but has become known to be associated with sudden, unexpect...

Journal: : 2022

Cardiac physiologic changes during pregnancy may cause risky delivery in patients with congenital cardiac anomalies. In this case, we present the anesthesia management emergency cesarean section a pregnant woman c-TGA who develop tamponade and sudden death risk due to pericardial effusion.

2013
Bilal Mirza

Anorectal malformations (ARM) are associated with a myriad of congenital anomalies. The prevalence rates of associated anomalies range from 20% to 80%, commonest being urogenital anomalies. Other important associations and syndromes include Down syndrome and VACTERL (vertebral, anorectal, cardiac, trachea-esophageal, renal, limb) anomalies [1]. ARM has rarely been described in association with ...

بابائی, احمد, طبیبان, ساسان, نباتی, مریم,

Accessory mitral valve tissue is a rare congenital malformation that has been reported in the literature in approximately 130 cases. This condition could be found isolated or in combination with other cardiac anomalies and is usually diagnosed in childhood. It is in differential diagnosis with other cardiac masses as tumors or vegetations. In this article a 27 year old asymptomatic female is p...

2007
Javier G. Castillo Sacha Salzberg Javier Sanz Farzan Filsoufi

Congenital coronary artery anomalies are sporadically discovered in patients undergoing coronary angiography and in autopsy series. Although most anomalies are clinically insignificant, some may become causes of cardiovascular morbidities and mortality. Diagnosis is commonly made with conventional coronary artery angiography. The current development of modern cardiac computed tomography allows ...

Journal: :journal of dentistry, tehran university of medical sciences 0
dana tahririan resident, department of pediatric dentistry, faculty of dentistry, isfahan university of medical sciences, isfahan, iran. alireza eshghi associate professor of pediatric dentistry, isfahan university of medical sciences, isfahan, iran. pirooz givehchian resident, department of prosthodontics, faculty of dentistry, isfahan university of medical sciences, isfahan, iran. mohammad ali tahririan assistant professor of orthopedics, isfahan university of medical science, isfahan, iran.

chondroectodermal dysplasia (ellis-van creveld syndrome) is a rare autosomal recessive congenital abnormality. this syndrome is characterized by a spectrum of clinical findings, among which chondrodystrophy, polydactyly, ectodermal dysplasia, and congenital cardiac anomalies are the most common. it is imperative to not overlook the cardiac complications in patients with this syndrome during den...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید