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diagnosis algorithm clinical differential congenital infant management tetralogy 21hydroxylasedeficiency 21ohd anatomy anomalies chest childhood circulation cxr dermatology diagram ebstein endocrinology
Ebstein Anomaly • Prevalence • Pathophysiology • Presentation • Physical Examination Findings • Initial Management •
Ebstein Anomaly ... Prevalence • Pathophysiology ... surgery for Ebstein anomaly ... diagnosis #management #cardiology ... #pediatrics #peds
Causes of Pediatric Wheezing - Differential Diagnosis Algorithm CXR Abnormal: • Pulmonary Sequestration • Congenital Adenoid Cystic
Causes of Pediatric ... Vascular Compression Syndrome ... • Structural Anomaly ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Causes of Sudden ... • Pulmonary Anomaly ... Sudden Infant Death Syndrome ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Causes of Congenital Anomalies - Differential Diagnosis Algorithm Malformation • Embryonic development failure or inadequacy (often multifactorial) Deformation
Causes of Congenital ... of Anomalies (Syndromic ... Congenital #Anomalies #Anomaly ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... Associated Genetic Syndromes ... diagnosis #management #cardiology ... #peds #pediatrics
Staphylococcal Scalded Skin Syndrome (SSSS) A 5-year-old girl presents to the ED with a rash that started
Staphylococcal Scalded Skin ... Syndrome (SSSS) ... #Syndrome #SSSS ... #Clinical #Photo ... #Peds #Pediatrics
Tetralogy of Falot on Chest X-Ray Tetralogy of Falot comprises four defects - 1. Ventricular septal defect (VSD) 2.
boot shaped heart caused ... common cardiac anomaly ... CXR #clinical #radiology ... #peds #pediatrics ... #cardiology #ToF
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
URT inflammation causes ... that persists as skin ... > Inflammation causes ... #Immunization #peds ... #pediatrics #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
with pigmented skin ... intra-abdominal masses ... defects of the skin ... #Examination #Peds ... #Pediatrics #Diagnosis
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