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Effect of digoxin, verapamil, and amiodarone
Effect of digoxin, verapamil, and amiodarone

... limitations, since congenital cardiac anomalies may cause alteration of the QRS, multiple accessory pathways may coexist as well as variable degrees of fusion between the normal and the abnormal pathway with superposition of the P wave on the delta waves.'3 Recent electrophysiological studies in chi ...
A case of 75-year-old survivor of unrepaired tetralogy of Fallot and
A case of 75-year-old survivor of unrepaired tetralogy of Fallot and

... shunt may damage the aortic cusps, whilst in TOF the output of both ventricles is ejected directly into the aorta, with no alteration of aortic valve function.10 Other reported causes of AR were a deformed aortic valve secondary to endocarditis and severe dilation of the aortic annulus.2 Aortic root ...
Transient Prolongation of QT Interval in a Neonate
Transient Prolongation of QT Interval in a Neonate

... The length of the QT interval may indicate prognosis. In one study, patients with a QTc less than 0.50 seconds eventually recovered with a normal QTc; those with a QTc greater than 0.60 seconds had severe arrhythmias ...
Advances in Perinatal Genetics
Advances in Perinatal Genetics

... • Genes and unknown environmental influences can interact to cause a specific birth defect • Many hereditary conditions are thought to be multifactorial in nature as well ...
A rare case of scimitar syndrome with horseshoe lung
A rare case of scimitar syndrome with horseshoe lung

... contrast-enhanced computed tomography (CT) scan of the chest was obtained. Coronal reconstruction of the CT scan showed a scimitar shaped vein running from the middle of the right lung towards the diaphragm and draining into the inferior vena cava (fig. 1a). Also visible was an anomalous midline pul ...
Correctable Cause of Dilated Cardiomyopathy in an Infant with
Correctable Cause of Dilated Cardiomyopathy in an Infant with

... A 2.5-month-old female patient, who had no previous symptoms, presented with distress, constant crying, feeding problems, tachypnea and sweating for 3-4 days. Teleradiography performed at a different center showed cardiomegaly, echocardiographic evaluation showed DCM. Following inconclusive metaboli ...
9/09 Aortic Regurgitation
9/09 Aortic Regurgitation

... despite severe aortic regurgitation Most common technique to visualize AR Sensitivity > 95% ...
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Diagnosis of valvular diseases

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TAVR - SCACVPR

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Supraventricular tachycardia from a left bundle

... although electrophysiological testing would be required to determine this. WPW is not a benign condition with instances of sudden death in individuals of WPW in both those symptomatic and asymptomatic. There is still often debate on the best treatment for cases of asymptomatic WPW syndrome as the ri ...
Sudden Death In the Structurally Normal Heart
Sudden Death In the Structurally Normal Heart

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Edwards syndrome
Edwards syndrome

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Пульсоксиметрия как скрининговый метод ранней диагностики

... Regional Perinatal Center from 01.12.2012 to 10.04.2013 performed screening measure blood oxygen saturation (SpO2) by pulse oximetry (pulse oximeter «Utas Um 300») at the age 24 - 48 hours of life. Saturation threshold is taken as 95% [AHA/AAP, 2009]; also accounted the difference between the right ...
Severe Aortic Stenosis and Severe Coarctation of the Aorta: A
Severe Aortic Stenosis and Severe Coarctation of the Aorta: A

... performed using the femoral artery, however, carotid and axillary cutdown is now being used with more success and less complications. Rossi and the group from Porto Alegre in Brazil found rates of femoral arterial occlusion as high as 40% (6). Over a 16-year period, a clear leg length discrepancy wa ...
CONGENITAL BICUSPID AORTIC VALVE – A CASE REPORT
CONGENITAL BICUSPID AORTIC VALVE – A CASE REPORT

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Guide to Marfan syndrome

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... blood flow and, in this instance, is usually quite loud due to the obstruction of the aortic valve. **Note: Puppies under 16 weeks of age sometimes demonstrate what is called a ‘physiological’ or ‘innocent’ murmur. These are not very loud and disappear as the puppy gets older; any murmur that persis ...
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Aortic Stenosis Client Handout PESC

... blood flow and, in this instance, is usually quite loud due to the obstruction of the aortic valve. **Note: Puppies under 16 weeks of age sometimes demonstrate what is called a ‘physiological’ or ‘innocent’ murmur. These are not very loud and disappear as the puppy gets older; any murmur that persis ...
syndrome
syndrome

... frequent congenital heart defects susceptibility to infections life expectancy is good the risk of Down syndrome increases with age after 40 years prenatal diagnosis (amniocentesis) is recommended for all pregnant women age 35 or older ...
16 (2), 2013 85-90 DOUBLE ANEUPLOIDY 48,XXY,+21
16 (2), 2013 85-90 DOUBLE ANEUPLOIDY 48,XXY,+21

... The occurrence of double aneuploidy of DS combined with KS is unclear, not to mention the double aneuploidy associated with CHD. Approximately 65 cases of double aneuploidy of XXY and trisomy 21 have been published since 1959, and there are only eight cases associated with CHD [1214], including our ...
A Case of Aortic Dissection With Fistula From Aorta to Right Ventricle
A Case of Aortic Dissection With Fistula From Aorta to Right Ventricle

... that time. A chest radiograph showed cardiomegaly with cardiothoracic index of 62%. Ventricular premature complex and left ventricular hypertrophy were noted on electrocardiogram. Esophagogastroscopy revealed no abnormal findings. Transthoracic echocardiography showed severely dilated aortic root an ...
Oral Manifestations in Ellis-van Creveld Syndrome: Report of Five
Oral Manifestations in Ellis-van Creveld Syndrome: Report of Five

... these oral abnormalities as they are of no specific type.17 Cardiac defects present in some EvC patients and require antibiotic coverage for the prevention of infectious endocarditis.5 Almost half of these patients die during childhood because of cardiorespiratory complications13; for this reason, t ...
Oral Manifestations in Ellis
Oral Manifestations in Ellis

... these oral abnormalities as they are of no specific type.17 Cardiac defects present in some EvC patients and require antibiotic coverage for the prevention of infectious endocarditis.5 Almost half of these patients die during childhood because of cardiorespiratory complications13; for this reason, t ...
Evaluation of Left Ventricle Systolic and Diastolic
Evaluation of Left Ventricle Systolic and Diastolic

... Iran J Pediatr. In Press(In Press):e5735. ...
Combined Aortic Valve Replacement and Coronary Artery Bypass
Combined Aortic Valve Replacement and Coronary Artery Bypass

... without clamping the aorta and aortic valve replacement. Aortic valve replacement and two distal coronary artery anastomoses to the left circumflex artery and obtuse marginal branch were performed under cardiac arrest during hypothermic perfusion with endoaortic balloon occlusion, followed by partia ...
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Turner syndrome



Turner syndrome (TS) also known as Ullrich–Turner syndrome, gonadal dysgenesis, and 45,X, is a condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary among those affected. Often, a short and webbed neck, low-set ears, low hairline at the back of the neck, short stature, and swollen hands and feet are seen at birth. Typically they are without menstrual periods, do not develop breasts, and are unable to have children. Heart defects, diabetes, and low thyroid hormone occur more frequently. Most people with TS have normal intelligence. Many, however, have troubles with spatial visualization such as that needed for mathematics. Vision and hearing problems occur more often.Turner syndrome is not usually inherited from a person's parents. No environmental risks are known and the mother's age does not play a role. Turner syndrome is due to a chromosomal abnormality in which all or part of one of the X chromosomes is missing or altered. While most people have 46 chromosomes, people with TS usually only have 45. The chromosomal abnormality may be present in just some cells in which case it is known as TS with mosaicism. In these cases, the symptoms are usually fewer and possibly none occur at all. Diagnosis is based on physical signs and genetic testing.No cure for Turner syndrome is known. Treatment, however, may help with symptoms. Human growth hormone injections during childhood may increase adult height. Estrogen replacement therapy can promote development of the breasts and hips. Medical care is often required to manage other health problems with which TS is associated.Turner syndrome occurs in between one in 2000 and one in 5000 females at birth. All regions of the world and cultures are affected about equally. People with TS have a shorter life expectancy, mostly due to heart problems and diabetes. Henry Turner first described the condition in 1938. In 1964, it was determined to be due to a chromosomal abnormality.
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