A5091327133- Congenital Heart Disease Studies
- Cardiac Arrhythmias and Treatments
- Vascular anomalies and interventions
- Coronary Artery Anomalies
- Pulmonary Hypertension Research and Treatments
- Cardiac Structural Anomalies and Repair
- Aortic Disease and Treatment Approaches
- Tracheal and airway disorders
- Cardiac Valve Diseases and Treatments
- Cardiovascular Effects of Exercise
- Abdominal vascular conditions and treatments
- Parathyroid Disorders and Treatments
- Dermatological and Skeletal Disorders
- Vascular Anomalies and Treatments
- Cardiovascular Issues in Pregnancy
- Cardiac tumors and thrombi
- Hypertrophic osteoarthropathy and related conditions
- Transplantation: Methods and Outcomes
- Kawasaki Disease and Coronary Complications
All India Institute of Medical Sciences
2023-2025
Kartagener syndrome (KS) is a rare autosomal recessive condition with triad of situs inversus, bronchiectasis, and sinusitis. In majority cases, the heart structurally normal; however, rarely intracardiac anomalies can be seen in patients KS such atrial or ventricular septal defects pulmonary stenosis. We present coexistence mesocardia, corrected transposition great arteries young adolescent male diagnosed on computed tomography angiography.
ABSTRACT Partial cavopulmonary shunt is an established procedure for patients with abnormal right ventricular (RV) physiology. Late failure of the Glenn usually due to further progression primary disease process. However, there may be surprises, as in our patient. We report 8-year-old child who was diagnosed tricuspid valve (TV) dysplasia borderline RV hypoplasia. He underwent TV repair a shunt. presented features heart after 6 years surgery. An echocardiographic evaluation suggested...
ABSTRACT Arterial desaturation following surgical repair of tetralogy Fallot (TOF) is rare. In most instances, it results from residual right ventricular outflow tract obstruction, causing right-to-left shunt across interatrial or interventricular communication. this report, we present an unusual scenario arterial due to a recanalized left cardinal vein in child with repaired TOF. We also discuss stepwise evaluation that led successful identification and occlusion the abnormal venous channel...
We present the case of a 4-year-old girl with tetralogy Fallot associated an incidentally detected isolation left brachiocephalic artery, no communication between it and pulmonary artery or ductus arteriosus. The highlights unusual association hemodynamic consequences condition.
Kawasaki disease, traditionally classified as medium vessel vasculitis, is known for the preferential involvement of coronary arteries. Infrequently, large systemic arteries might be involved and may affect prognosis. Here, we present an infant with disease who had extensive vessels such abdominal aorta extremities, along giant artery aneurysms.
Generalized arterial calcification of infancy is a rare entity with poor fetal and postnatal outcomes high morbidity in survivors. Half the cases are diagnosed intrauterine due to hemodynamic compromise, associated manifestations pose unique management challenges. We hereby report an account diagnosis referral for hydrops evaluation management.
"Truncus arteriosus with isolated origin of left subclavian artery from the pulmonary trunk." Acta Cardiologica, ahead-of-print(ahead-of-print), pp. 1–2 Disclosure statementNo potential conflict interest was reported by author(s).