15 results
Ebstein Anomaly
 • Prevalence
 • Pathophysiology
 • Presentation
 • Physical Examination Findings
 • Initial Management
 •
Prevalence • Pathophysiology ... and Adults • Cone ... diagnosis #management #cardiology ... #pediatrics #peds
Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... Exam The scarf sign ... #clinical #video ... hypotonia #hypotonic #peds ... #pediatrics #tone
Tone - Leg Traction on Physical Exam
Leg traction is done by holding the leg by the
Tone - Leg Traction ... on the leg is a sign ... Traction #Lower #Extremity ... PhysicalExam #clinical #video ... #peds #pediatrics
Total Anomalous Pulmonary Venous Return (TAPVR)
 • Introduction
 • Classification
 • Pathophysiology of TAPVR
 • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... diagnosis #management #cardiology ... #peds #pediatrics
Lower Extremity Tone on Physical Exam
Assessing motor function of the lower extremities begins with passive range
Lower Extremity ... Tone on Physical ... LowerExtremity #tone ... PhysicalExam #clinical #video ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
While the pathophysiology ... Video by Dr. ... Meningitis #Clinical #Video ... #PhysicalExam #Pediatrics ... #Peds
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... Infertility • Decr Bone ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Pediatric Elbow Injuries - Elbow Xrays

Check the fat pads on the lateral projection:
1. A displaced anterior
Pediatric Elbow ... Check the fat pads ... fat pad (sail sign ... Injuries #Xrays #Radiology ... #peds #Pediatrics
Tone - Leg Recoil on Physical Exam
To test leg recoil, the legs are fully flexed on
Tone - Leg Recoil ... Recoil #Lower #Extremity ... #tone #Newborn ... PhysicalExam #clinical #video ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics