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peds differential epilepsy newborn seizures 21hydroxylasedeficiency 21ohd abuse anemia aorta brue chest clinical coarctation disease endocrinology epilepsies event examination figure3
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Unexpected Death in Infancy ... Illness Sudden Infant ... #Infant #Differential ... #Diagnosis #Algorithm ... Pediatrics
Causes of Pediatric Spells - Differential Diagnosis Algorithm Neonates and Infant Spells: • Benign Sleep Myoclonus •
Causes of Pediatric ... and Infant Spells ... Syndrome Older Infants ... #Algorithm #Causes ... #Peds #Pediatrics
Causes of anemia in infants & children #Diagnosis #Peds #Pediatrics #Differential #Anemia #Causes #Algorithm
Causes of anemia ... in infants & children ... #Diagnosis #Peds ... #Pediatrics #Differential ... #Algorithm
Causes of Pediatric Seizures - Differential Diagnosis Algorithm Infantile: • Benign Focal Epilepsy of Infancy • West
Causes of Pediatric ... Focal Epilepsy of Infancy ... Neonates and Infant ... #Algorithm #Causes ... #Peds #Pediatrics
Causes of Pediatric Stridor - Differential Diagnosis Algorithm Present Since Infancy with No Respiratory Distress: • Laryngomalacia Present
Causes of Pediatric ... Since Infancy with ... Present Since Infancy ... #Algorithm #Causes ... #Peds #Pediatrics
Causes of Unprovoked Pediatric Seizures - Epilepsy Syndromes - Differential Diagnosis Algorithm Infantile: • Benign
Causes of Unprovoked ... Pediatric Seizures ... Focal Epilepsy of Infancy ... #Algorithm #Causes ... #Peds #Pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Algorithm Cardiac ... Breathing • Apnea of Infancy ... #Algorithm #Causes ... #Peds #Pediatrics
Standardized Physical Abuse Guideline <6 months of age • Social work consult • Skeletal survey • Head
Head CT, AST, ALT ... • Troponin for infants ... > 80, signs of chest ... #Workup #Peds #Pediatrics ... #Diagnosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... , 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 ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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