نتایج جستجو برای: congenital cardiac disease

تعداد نتایج: 1770330  

Journal: :British heart journal 1971
A U Antia A O Williams

The present study of 47 necropsy cases of congenital heart disease has revealed that cardiac defects occur as frequently in the African as in the non-African. The types of congenital heart disease and the associated non-cardiac malformations are similar to what has been described in non-Africans. Tetrad of Fallot was the commonest type of multiple defect and ventricular septal defect the most c...

Journal: :JPMA. The Journal of the Pakistan Medical Association 2011
Nuruddin Badruddin Mohammed Anandakumar Chinnaiya

Congenital cardiac anomalies are the most common anomalies, with an estimated incidence of about 4-13 per 1000 live births. Proper perinatal and neonatal management is dependent upon accurate prenatal diagnosis. Approximately 10% of foetuses with cardiac abnormalities have identified risk factors; hence, most of the anomalies occur in pregnancies without prenatal risk factors. Foetal echocardio...

Journal: :Kathmandu University medical journal 2016
A Joshi R Pb Shrestha P S Shrestha S Dangol N C Shrestha P Poudyal A Shrestha

Background Congenital Heart Disease and Rheumatic Heart Disease are the most common childhood cardiac disease encountered in developing countries. Objective To study the pattern and the prevalence of cardiac diseases, its age wise distribution and to determine their risk factors for mortality in children presented to Dhulikhel Hospital, Kathmandu University Hospital. Method A study of cardiac d...

Journal: :Journal of congenital cardiology 2021

Abstract Approximately 50% of newborns with Down syndrome have congenital heart disease. Non-cardiac comorbidities may also be present. Many the principles and strategies perioperative evaluation management for patients disease apply to those syndrome. Nevertheless, careful planning cardiac surgery is required, evaluating both noncardiac disease, consideration risk pulmonary hypertension. In th...

H Mottaghi Moghadam M Horri N Motevalli Haghi R Erfani Sayyar S Elmi Sam Elmi Sh Rahmani

Introduction: Infective endocarditis is a rare, fatal ,with high morbidity in children, Since infective endocarditis in children was not assessed in our conditions so our study was attempted.   Material and Methods: This cross-sectional  study  include 19 patients less than 18 years old  with endocarditis   were hospitalized in the Department of Pediatric Cardiology( University of Mashhad...

Journal: :iranian journal of otorhinolaryngology 0
shahin abdollahi fakhim department of otorhinolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran. nikzad shahidi department of otorhinolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran. alireza lotfi department of otorhinolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran.

introduction: orofacial clefts are among the most common congenital anomalies. patients presenting with orofacial clefts often require surgery or other complex procedures. a cleft lip or palate can be a single anomaly or a part of multiple congenital anomalies. the reported prevalence of cleft disease and associated anomalies varies widely across the literature, and is dependent on the diagnost...

Journal: :Heart 2012
Michael Burch Nathalie Dedieu

This Almanac highlights recent papers on congenital heart disease in the major cardiac journals. Over 100 articles are cited. Subheadings are used to group relevant papers and allow readers to focus on their areas of interest, but are not meant to be comprehensive for all aspects of congenital cardiac disease.

Journal: :Congenital Heart Disease 2022

Objective: Junctional ectopic tachycardia is common after cardiac surgery for congenital heart disease. However, its incidence and related risk factors in infants are not well known. The objective of this study was to determine the overall junctional neonates infants. Methods: We enrolled a total 271 patients aged

Journal: :Interactive CardioVascular and Thoracic Surgery 2009

Journal: :international journal of reproductive biomedicine 0
katayoon etemadi behnaz basir safieh ghahremani

background: 49, xxxxy syndrome is a rare sex chromosomal disorder, occurring in 1 per 85,000-100,000 male births. the classical phenotype is ambiguous genitalia, facial dysmorphism, mental retardation and a combination of cardiac, skeletal and other malformations. case: a two month-old boy with intrauterine growth restriction (iugr) and low birth weight, facial dysmorphism, clinodactyly in feet...

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