8 results
Tetralogy of Fallot 

1. Right ventricular outflow tract obstruction 

2. Right ventricular hypertrophy 

3. Ventricular septal
Tetralogy of Fallot ... @Roshcast #Tetralogy ... #Fallot #Peds # ... Pediatrics #Cardiology ... #Signs #Symptoms
Tetralogy of Falot on Chest X-Ray
Tetralogy of Falot comprises four defects -
1. Ventricular septal defect (VSD)
2.
Tetralogy of Falot ... on Chest X-Ray Tetralogy ... 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 ... #Tetralogy #Fallot ... #ChestXRay #Clinical ... #Radiology #CXR ... #Peds #Pediatrics
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... Pale or Mottled Skin ... PhysicalExam #Signs #Symptoms ... #Dehydration #Peds ... #Pediatrics
Scurvy (Vitamin C Deficiency) - Diagnosis and Management

Vitamin C is required for hydroxylation of proline residues
integrity of: • Skin ... poor nutrition Clinical ... Psychiatric symptoms ... : • Petechia • ... • Petechiae, purpura
Diagnosis of IgA Vasculitis (Henoch-Schönlein Purpura) - French Vasculitis Study Group 

1) Suggestive clinical manifestations
Henoch-Schönlein Purpura ... 1) Suggestive clinical ... individuals - Clinical ... #Rheumatology #Peds ... #Pediatrics
Pediatric Parasomnias and Nightmares: Pathogenesis and clinical findings

Parasomnias - Micro-arousal episodes during SWS ->
Intense activation of
Pediatric Parasomnias ... Pathogenesis and clinical ... Speech • Flushed skin ... #Peds #pathophysiology ... #symptoms #pharmacology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... cold & mottled skin ... endocrinology #peds ... #pediatrics