12 results
Validation of the “Step-by-Step” Approach in the Management of Young Febrile Infants
Visual Abstract by Dr. Kirsty
Management of Young Febrile ... Infants Visual ... pubmed/27382134 #EBM ... #Peds #Pediatrics ... #Infant #Risk #
Decision Aid - What is the risk of serious infection in febrile infants (<60 days old)?

Reference:
infants (<60 days ... Reference: JAMA Pediatr ... #Infant #Peds # ... Pediatrics #DecisionAid ... #Stewardship #EBM
Causes of Pediatric Stridor - Differential Diagnosis Algorithm
Present Since Infancy with No Respiratory Distress:
 • Laryngomalacia
Present
Causes of Pediatric ... Present Since Infancy ... Present Since Infancy ... Acute Onset Febrile ... #Peds #Pediatrics
The Febrile Child - some diagnostic clues to evaluating the febrile child.

#Febrile #Fever #Evaluation #Assessment #Signs
The Febrile Child ... some diagnostic clues ... Evaluation #Assessment #Signs ... PhysicalExam #Diagnosis #Peds ... #Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... Focal Epilepsy of Infancy ... Infection: • Febrile ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Tetralogy of Fallot 

1. Right ventricular outflow tract obstruction 

2. Right ventricular hypertrophy 

3. Ventricular septal
Overriding aorta ... Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms
The Febrile Infant Step-by-Step Algorithm
This is an algorithm developed by European emergency physicians to identify low-risk
The Febrile Infant ... identify low-risk infants ... 46.9% #Diagnosis #EBM ... #Management #Pediatrics ... #Peds #Febrile
Tetralogy of Falot on Chest X-Ray
Tetralogy of Falot comprises four defects -
1. Ventricular septal defect (VSD)
2.
Overriding aorta ... boot shaped heart caused ... CXR #clinical #radiology ... #peds #pediatrics ... #cardiology #ToF
Figure of 3 Sign - Coarctation of the Aorta on Chest X-Ray

The figure of 3 sign
distal aortic arch caused ... rib notching is caused ... seen in infancy ... XRay #clinical #radiology ... #pediatrics
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 ... endocrinology #peds ... #pediatrics