26 results
Paradoxical Breathing on Physical Exam

Paradoxical breathing is often a sign of breathing problems. It causes the
breathing is often a sign ... It causes the chest ... respiratory #clinical #video ... #pulmonary #peds ... #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... Video by Dr. ... #PhysicalExam #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
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
Gowers' Sign on Physical Exam

Caused by proximal muscle weakness typically seen in muscular dystrophy

#Gowers #Sign #PhysicalExam
Gowers' Sign on ... Physical Exam Caused ... #Sign #PhysicalExam ... neurology #clinical #video ... #pediatrics #muscular
Childhood Immunization Schedule: Why we immunize
 • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
asymmetric reduction in tone ... Maternal viremia causes ... > Inflammation causes ... #Immunization #peds ... #pediatrics #pathophysiology
Tone - Leg Traction on Physical Exam
Leg traction is done by holding the leg by the
on the leg is a sign ... Leg #Traction #Lower ... #Extremity #tone ... PhysicalExam #clinical #video ... #peds #pediatrics
Lower Extremity Tone on Physical Exam
Assessing motor function of the lower extremities begins with passive range
Lower Extremity ... Tone on Physical ... function of the lower ... PhysicalExam #clinical #video ... #peds #pediatrics
Galant Reflex on Physical Exam

The Galant reflex is present at birth and remains until the 2nd
possible change in tone ... persistent in cases ... PhysicalExam #clinical #video ... #Neurology #Peds ... #Pediatrics #Normal
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics