نتایج جستجو برای: congenital heart malformation

تعداد نتایج: 493580  

2015
Kinue Katano Yutaka Takeda Mayumi Sugiura-Ogasawara

Uterine arteriovenous malformation (AVM) is rare but it can cause life-threatening genital bleeding. Conservative therapy with GnRHa can be a useful option for treating a uterine AVM presenting with a congenital heart disease shunt in hemodynamically stable patients.

Journal: :Indian heart journal 2001
S S Kothari N Naik R Juneja A Saxena

In neonates, aneurysm of the vein of Galen often masquerades as cyanotic congenital heart disease. We report 4 cases of neonates presenting with malformation of the vein of Galen at our insititution. An increased awareness of this entity seems warranted.

Journal: :McGill Journal of Medicine : MJM 2008
Sherif E Moustafa Jacques Lesperance Jean-Lucien Rouleau Gilbert Gosselin

Shone's anomaly, a congenital cardiac malformation complex, consists of multiple levels of left heart obstruction. A rare case of an incomplete form of this anomaly discovered incidentally during cardiac catheterization for an unrelated event is described.

اسلامی, ابوالقاسم, رودپیما, شهلا,

Noonan syndrome is a genetic condition inherited by an autosomally dominant manner, characterised by congenital heart disease, short stature, abnormal facies and the somatic feature of Turner's syndrome, but a normal karyotype. Noonan syndrome affects approximately 1 in 1500 live births. Congenital heart disease occurs in 35-50% of patients diagnosed with noonan syndrome. The most common cardia...

Journal: :The Journal of the Association of Physicians of India 2016
J Rajendra Kumar Mamta B Kumbhare P Goutham Kumar T Vishal Goud

An accessory coronary cusp in aortic valve is a rare congenital cardiovascular malformation with an estimated incidence of 0.003 to 0.043% of all congenital heart disease. It is also describe as a quadricuspid aortic valve (QAV). Several different anatomical variations of quadricuspid aortic valve have been described. Current technology enables noninvasive diagnosis in most cases. Here we repor...

Journal: :Circulation 1976
J J Nora A H Nora

The risk of recurrence of a congenital cardiovascular malformation in a child having one parent with congenital heart disease has been determined for each of the seven most common anomalies presently compatible with survival to reproductive age. The range of risk is 2.5% to 4.3% depending on the lesion. This is within the range of expectation for the model of multifactorial inheritance previous...

Abbas Alizadeh Kaseb Ahmad Shah Farhat, Ashraf Mohammadzadeh, Fatemeh Khorakian Reza Saeidi,

Vein of Galen aneurysmal malformation (VGAM) is a rare congenital malformation, accounting for less than 1% of cerebrovascular abnormalities. The majority of reported cases have been associated with congestive heart failure (CHF) in the neonatal period. Herein, we present a case of VGAM, diagnosed at 37 weeks of gestation during the intrauterine life Case report: A full-term female newborn pre...

Journal: :British heart journal 1971
T J David

The palmar dermatoglyphs of 800 patients with anatomically proven congenital heart disease were compared with prints from 1000 controls. A review of the previous studies revealed major technical deficiencies, and the present study failed to confirm most of the previously reported positive findings. An overall increase in the incidence of hypothenar patterns was found, probably explaining the pr...

Congenital cystic Adenomatoid malformation is a rare developmental abnormality of the lung occuring in 1-4/100000 live births.In most cases the outcome with CCAM in fetus is very good,while in some cases the outcome is very bad and can be life threatning for the fetus.we report here a case of 40 day old female infant who presented with worsening respiratory distress since birth and x ray and CT...

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 ...

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