8 results
diagnosis tetralogy 21hydroxylasedeficiency 21ohd anomalous aorticvalve arteriosus bicuspid chest clinical cxr ebstein endocrinology fallot falot praderwilli pulmonary radiology return stenosis
Ebstein Anomaly • Prevalence • Pathophysiology • Presentation • Physical Examination Findings • Initial Management •
Prevalence • Pathophysiology ... Findings • Initial Management ... #diagnosis #management ... #cardiology #pediatrics ... #peds
Aortic Stenosis & Bicuspid Aortic Valve (AS) • Introduction & Pathophysiology • Classifications • Epidemiology •
Introduction & Pathophysiology ... Pre-operative Management ... Post-operative Management ... #AorticValve #cardiology ... #peds #pediatrics
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... Fallot #diagnosis #management ... #cardiology #peds ... #pediatrics #treatment
Truncus Arteriosus • Basic Information • Embryology • Associated anomalies • Pathophysiology/Presentation • Pre-operative management •
anomalies • Pathophysiology ... Pre-operative management ... vasculature, right aortic ... #cardiology #peds ... #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
Tetralogy of Falot on Chest X-Ray Tetralogy of Falot comprises four defects - 1. Ventricular septal defect (VSD) 2.
Overriding aorta ... common cardiac anomaly ... which is a common complication ... #peds #pediatrics ... #cardiology #ToF
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... Pre-Operative Management ... #cardiology #peds ... #pediatrics #summary
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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