12 results
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
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
Total Anomalous Pulmonary Venous Return (TAPVR)
 • Introduction
 • Classification
 • Pathophysiology of TAPVR
 • Presentation
Diagnosis • Chest XRay ... 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.
Falot on Chest X-Ray ... #Falot #Chest #XRay ... #CXR #clinical ... #radiology #peds ... #pediatrics #cardiology
Hand XRay - Bone Changes Over Time

Dr. Shadowgazer @DShadowgazer

#HandXRay #Progression #Timeline #HandBones #Bony #Changes #Clinical #Peds
Hand XRay - Bone ... Bony #Changes #Clinical ... #Peds #Pediatrics ... #Radiology
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Pediatric Elbow Injuries - Elbow Xrays

Check the fat pads on the lateral projection:
1. A displaced anterior
Pediatric Elbow ... Injuries - Elbow Xrays ... fat pad (sail sign ... #Radiology #peds ... #Pediatrics #clinical
Tetralogy of Fallot - Chest XRay

An 18-month-old male presents with his parents who have noticed that
Fallot - Chest XRay ... 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
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