18 results
cardiology treatment differential genetics pneumonia summary tetralogy 21hydroxylasedeficiency 21ohd acquired adult algorithm alkaptonuria anomalous arteriosus atrioventricular blackurine cap causes chf
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Tetralogy of Fallot ... #Tetralogy #Fallot ... #Peds #Pediatrics ... #Cardiology #Signs ... #Symptoms #Diagnosis
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... #diagnosis #differential ... #neonatal #pediatrics ... #adult #peds #pulmonary
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
Tetralogy of Fallot ... • Incidence • Pathophysiology ... #diagnosis #management ... #cardiology #peds ... #pediatrics #treatment
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Total Anomalous Pulmonary ... Classification • Pathophysiology ... PVO Present • Diagnosis ... Classic “snowman sign ... #peds #pediatrics
Atrioventricular Septal Defect aka AV canal defect aka endocardial cushion defect • Epidemiology and Associations • Embryology
Physical Exam • Pathophysiology ... • Long Term Follow ... endocardial #cushion #diagnosis ... #management #peds ... #pediatrics #cardiology
Truncus Arteriosus • Basic Information • Embryology • Associated anomalies • Pathophysiology/Presentation • Pre-operative management •
anomalies • Pathophysiology ... Pre-operative management ... Cardiomegaly, increased pulmonary ... Truncus #Arteriosus #diagnosis ... #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... sleep apnea, cor pulmonale ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Pott's Disease in Tuberculosis - Diagnosis and Management Summary Epidemiology: - Typically from TB endemic areas -
cases Clinical Signs ... years - May have signs ... pulmonary TB PE ... decreased reflexes Pathophysiology ... for concomitant pulmonary
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Croup Diagnosis and Management Pearls Common childhood illness, usually viral and self limiting. Characterised by a seal-like
Croup Diagnosis ... and Management Pearls ... see-saw breathing, pallor ... #Management #pediatrics ... #peds
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