نتایج جستجو برای: extra cardiac anomalies

تعداد نتایج: 384316  

2013
Allan Johansen Milan Lomsky Oke Gerke Lars Edenbrandt Lena Johansson Gunhild Hansen Birgitte Jensen Maria Sallerup Reid Lise-Lott Johansson Camilla Olofsson David Minarik Karin Nyström Per Wollmer Elin Trägårdh

BACKGROUND Technetium-labeled agents, which are most often used for assessing myocardial perfusion in myocardial perfusion scintigraphy (MPS), are cleared by the liver and excreted by the biliary system. Spillover from extra-cardiac activity into the myocardium, especially the inferior wall, might conceal defects and lower the diagnostic accuracy of the study. The objective was to determine rul...

Journal: :Journal of medical genetics 1968
A B Mukherjee M W Partington N E Simpson K A Walmsley

In man there are three well-known syndromes that are associated with an extra autosome. These are Down's syndrome (mongolism) with 21-trisomy (Lejeune, Gautier, and Turpin, 1959; Jacobs et al., 1959; Book, Fraccaro, and Lindsten, 1959), 13-15 trisomy (Patau et al., 1960), and 17-18 trisomy (Edwards et al., 1960; Smith et al., 1960). There have been five previously reported patients with a small...

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 ...

Journal: :Interactive cardiovascular and thoracic surgery 2011
Anthony Azakie Natalie C Johnson Petros V Anagnostopoulos Glenn D Egrie Michael J Lavrsen Anil Sapru

Low birth weight (LBW) is a risk factor for mortality in neonatal and infant heart surgery. The purpose of this study was to determine the contemporary outcomes and risk factors of cardiac surgery in low weight babies. The records of 75 consecutive infants weighing <2.5 kg having heart surgery were reviewed. The median weight was 2100 g (range 800-2500 g) and median age was 11 days (range 2-86 ...

Journal: :veterinary research forum 0
belal hassanzadeh central lab, faculty of veterinary medicine, university of tabriz, tabriz, iran arefeh rahemi navid institute of radiology and sonography, tabriz, iran

developing supernumerary limbs is a rare congenital condition that only a few cases have been documented. depending on the cause and developmental conditions, they may be single, multiple or complicated, and occur as a syndrome or associated with other anomalies. polymelia is defined as the presence of extra limb(s) which have been reported in human, mouse, chicken, calf and lamb. it seems that...

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