11 results
Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... laterally across the chest ... #clinical #video ... hypotonia #hypotonic #peds ... #pediatrics #tone
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... dehydration in an infant ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Peds #Pediatrics
Tetralogy of Fallot 

1. Right ventricular outflow tract obstruction 

2. Right ventricular hypertrophy 

3. Ventricular septal
Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms
Coins on Chest XRay - Trachea vs Esophagus

Coins in the sagittal plane on X-ray are more
Coins on Chest XRay ... Trachea #Esophagus #Peds ... #Pediatrics #CXR ... #Radiology #Comparison ... #Clinical
Total Anomalous Pulmonary Venous Return (TAPVR)
 • Introduction
 • Classification
 • Pathophysiology of TAPVR
 • Presentation
Diagnosis • Chest ... Classic “snowman sign ... diagnosis #management #cardiology ... #peds #pediatrics
Tetralogy of Falot on Chest X-Ray
Tetralogy of Falot comprises four defects -
1. Ventricular septal defect (VSD)
2.
Tetralogy of Falot on Chest ... develops after birth Chest ... #XRay #CXR #clinical ... #radiology #peds ... #pediatrics #cardiology
Tetralogy of Fallot - Chest XRay

An 18-month-old male presents with his parents who have noticed that
Tetralogy of Fallot - Chest ... A chest x-ray is ... Fallot #ChestXRay #Clinical ... #Radiology #CXR ... #Peds #Pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection: 
 - Bacterial: Streptococcus
Pathogenesis and Clinical ... , mastoiditis, febrile ... pathophysiology #diagnosis #symptoms ... #signs #peds #pediatrics
Pediatric Elbow Injuries - Elbow Xrays

Check the fat pads on the lateral projection:
1. A displaced anterior
Pediatric Elbow ... fat pad (sail sign ... Injuries #Xrays #Radiology ... #peds #Pediatrics ... #clinical
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics