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diagnosis causes algorithm cardiology genetics management symptoms 21hydroxylasedeficiency 21ohd adult anomalous baby blue color cyanosis diagram distress endocrinology fontan gray
Causes of Pediatric Wheezing - Differential Diagnosis Algorithm CXR Abnormal: • Pulmonary Sequestration • Congenital Adenoid Cystic
Causes of Pediatric ... Wheezing - Differential ... Sequestration • Congenital ... Algorithm #Causes #Peds ... #Pediatrics #Pulmonary
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
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Total Anomalous Pulmonary ... Classification • Pathophysiology ... Classic “snowman sign ... management #cardiology #peds ... #pediatrics #summary
Causes of Cyanosis in the Newborn - Differential Diagnosis Algorithm Peripheral Only: • Poor Perfusion • Acrocyanosis Hemoglobinopathy:
the Newborn - Differential ... Hemoglobinopathy: • Congenital ... Total Anomalous Pulmonary ... Algorithm #Causes #Peds ... #Pediatrics
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Infancy (SUDI) - Differential ... Diagnosis Algorithm Congenital ... Neurologic Anomaly • Pulmonary ... Algorithm #Causes #Peds ... #Pediatrics
Undifferentiated critical congenital heart disease: Patterns of Presentation Pink baby: • Presents at 1-6 mo
Undifferentiated critical congenital ... if cardiac or pulmonary ... #presentation #Differential ... Blue #Gray #Baby #Peds ... #Pediatrics #Color
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... sleep apnea, cor pulmonale ... 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
also known as "congenital ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
-55; f 50-60y (hormonal ... survival is 93-95% Pathophysiology ... Pulmonary: dyspnea ... nodules; anterior/posterior ... Diagnosis #Management #Signs
Fontan Procedure Schematic A Fontan is done in most children (approximately 90%) who effectively have a single
valvular atresia or a congenital ... flow into the pulmonary ... Schematic #Diagram #congenital ... #Cardiology #Peds ... #Pediatrics #Pathophysiology
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