Ebsteins anomaly is a rare complex congenital heart disorder with malformation of the tricuspid valve and right ventricle associated to left shunt. Severity can range from asymptomatic severely debilitated. We have discussed case 12-year-old female patient for cerebral abscess drainage.

holt-oram syndrome (hos) is a developmental disorder inherited in an autosomal-dominant pattern. affected organs are the heart and forelimbs with upper extremity skeletal defects and congenital heart malformation. in this study we present three cases of hos in the same family. in one of these three individuals we detected a transition of c to t (ctg-gtt, v205v) in exon 7 of the tbx5 gene. this ...

now-a-days truncus arteriosus has been known as “common arterial trunk” (cat) and is an uncommon congenital cardiac defect presenting in about 1-3% congenital heart disease. environmental and genetic factors effects on incidence of cat and other conotruncal anomalies. the majority patients with cat and 22q11 deletion have other anomalies such as hypoplasia or aplasia of the thymus or parath...

One of the most common cardiovascular diseases is congenital heart disease (CHD) and adult (ACHD) or CHD in patients. The chronic effects illness, surgery, hospitalization certain stages life can have significant impacts on a patients psychology quality life. This study aims to discover relationship between psychological disorders ACHD at Integrated Heart Service Center, Dr. Soetomo General Aca...

Noonan’s syndrome is a polymorphic disorder with some facial features, congenital heart defects, cryptorchidism, etc., and also associated autoimmune diseases, lymphatic dysplasias. Here we are reporting nine years old boy Noonan's who has hepatomegaly persistently raised hepatic enzymes, which remained unexplained.
 TAJ 2022; 35: No-1: 137-140

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...

Congenital left atrial wall aneurysm is a rare disorder that occurs in wide range of age groups from infancy to adulthood. Here, we present case congenital was detected 19-year-old man who surgically treated. Although the patient asymptomatic without any pre-existing conditions, chest radiography performed as part routine health examination abnormalities heart. Contrast-enhanced computed tomogr...

* Four cardiovascular abnormalities account for the great majority of reported cases of sudden cardiac death in young athletes: hypertrophic cardiomyopathy (a pathologically enlarged heart), congenital (inherited) abnormalities of the coronary arteries, dissecting aortic aneurysms (bulging of the aorta with blood passing between layers of the arterial wall) in athletes with Marfan syndrome (a c...

conclusions the right ventricular outflow tract palliation in children with cyanotic chd leads to long-term favorable outcome regarding improvement in oxygen saturation, increase in z score of both left and right pulmonary arteries and also considerable decrease in spell. also, death and complications are rare following rvot palliation. background the right ventricular outflow tract (rvot) pall...