21 results
Ossification of Carpal Bones

It’s always tricky to remember the age of ossification of the carpal bones
Ossification of ... interpreting a Pediatric ... -6-7 years for Triquetral ... Wrist #Diagnosis #Peds ... #Pediatrics
Bronchiolitis - Pathophysiology and Clinical Features

#Pediatrics #Peds #Pathophysiology #Bronchiolitis
Bronchiolitis - Pathophysiology ... and Clinical Features ... #Pediatrics # ... Peds #Pathophysiology
Pediatric Skull Fracture with Associated Hematoma on POCUS

Working with the challenges of risk stratification, management of
Pediatric Skull ... management of peds ... Hematoma #POCUS #Peds ... #Pediatrics #Clinical ... #Ultrasound
Aortic Stenosis & Bicuspid Aortic Valve (AS)
 • Introduction & Pathophysiology
 • Classifications
 • Epidemiology
 •
Introduction & Pathophysiology ... Epidemiology • Clinical ... AorticValve #cardiology #peds ... #pediatrics
Pediatric Parasomnias and Nightmares: Pathogenesis and clinical findings

Parasomnias - Micro-arousal episodes during SWS ->
Intense activation of
Pediatric Parasomnias ... Pathogenesis and clinical ... Parasomnias #Nightmares #Pediatrics ... #Peds #pathophysiology
Figure 53 – Longitudinal (left) and transverse (right) images from an ultrasound of the pylorus demonstrate
images from an ultrasound ... pyloric stenosis by ultrasound ... #Clinical #POCUS ... #Peds #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection: 
 - Bacterial: Streptococcus
Pathogenesis and Clinical ... #OtitisMedia #pathophysiology ... symptoms #signs #peds ... #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
While the pathophysiology ... Sign #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics