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cardiology diagnosis signs management clinical cxr genetics 21hydroxylasedeficiency 21ohd anomalous atrioventricular birthweight chest chestxray cushion defect dehydration endocardial endocrinology falot
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Tetralogy of Fallot ... @Roshcast #Tetralogy ... #Fallot #Peds # ... Pediatrics #Cardiology ... #Signs #Symptoms
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
Tetralogy of Fallot ... • Incidence • Pathophysiology ... #Fallot #diagnosis ... #management #cardiology ... #peds #pediatrics
Tetralogy of Falot on Chest X-Ray Tetralogy of Falot comprises four defects - 1. Ventricular septal defect (VSD) 2.
Tetralogy of Falot ... on Chest X-Ray Tetralogy ... of Falot comprises ... CXR #clinical #radiology ... #peds #pediatrics
Summary of problems of Very Low Birthweight Infants #Premature #Low #Birthweight #Peds #Pediatrics #Problems #Signs #Symptoms #Presentation
Low Birthweight Infants ... #Birthweight #Peds ... #Pediatrics #Problems ... #Signs #Symptoms
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
dehydration in an infant ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Infant #Dehydration ... #Peds #Pediatrics
Tetralogy of Fallot - Chest XRay An 18-month-old male presents with his parents who have noticed that
Tetralogy of Fallot ... #Tetralogy #Fallot ... ChestXRay #Clinical #Radiology ... #CXR #Peds #Pediatrics
Atrioventricular Septal Defect aka AV canal defect aka endocardial cushion defect • Epidemiology and Associations • Embryology
Physical Exam • Pathophysiology ... • Long Term Follow ... diagnosis #management #peds ... #pediatrics #cardiology
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... diagnosis #management #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 ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
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