10 results
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Unexpected Death in Infancy ... Illness Sudden Infant ... SuddenDeath #Unexpected #Infancy ... #Infant #Differential ... Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Focal Epilepsy of Infancy ... • Tumours • Congenital ... Neonates and Infant ... Syndrome Older Infants ... #Causes #Peds #
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Cardiac: • Congenital ... Heart Disease ... Breathing • Apnea of Infancy ... #Causes #Peds # ... Pediatrics
Congenital Heart Disorders - Classification and Differential Algorithm

- Amy Chung, MD, MSc @AmyChung 

#Congenital #Heart #Disorders
Congenital Heart ... #Heart #Disorders ... #Diseases #Classification ... #Diagnosis #Peds ... #Pediatrics #Cardiology
Simplified Diagnosis of Metabolic Disorders
#Diagnosis #Peds #Pediatrics #Inherited #Congenital #Metabolism #Metabolic #Diseases #Disorders #Ketones #Ammonia #Differential
#Diagnosis #Peds ... #Pediatrics #Inherited ... #Congenital #Metabolism ... #Metabolic #Diseases ... #Differential #Algorithm
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic Infant ... Differential Diagnosis Algorithm ... #Hypotonic #Infant ... #Causes #Peds # ... Pediatrics
American College of Critical Care Medicine algorithm for time-sensitive, goal-directed stepwise management of hemodynamic support in
Care Medicine algorithm ... hemodynamic support in infants ... 70% (* except congenital ... #CriticalCare #Peds ... #Pediatrics #Sepsis
Causes of Failure to Thrive - Differential Diagnosis Algorithm
Adequate Calorie Consumption
 - Increased Losses:
• Liver Disease ... • Metabolic Disorders ... Esophagitis • Congenital ... #Causes #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 ... deficiencies present in infants ... , vomiting • Late ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... , elevation of ALT ... #Diagnosis #Peds ... #Pediatrics #Kawasaki ... #Algorithm