24 results
Typical Clinical Features of Major Causes of Acute Chest Discomfort

#ChestPain #Features #Signs #Symptoms #Comparison #Table #Characteristics
Typical Clinical ... Features of Major Causes ... of Acute Chest ... ChestPain #Features #Signs ... #Symptoms #Comparison
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
Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... Exam The scarf sign ... #Scarf #Sign #PhysicalExam ... #clinical #video ... #pediatrics #tone
Windlass Test for Plantar Fasciitis

Passive extension of the great toe with the ankle in dorsiflexion. A
extension of the great toe ... A positive sign ... plantar fascia symptoms ... #clinical #video ... #msk #sports #orthopedics
Windlass Test for Plantar Fasciitis

Passive extension of the great toe with the ankle in dorsiflexion. A
extension of the great toe ... A positive sign ... plantar fascia symptoms ... #clinical #video ... #msk #sports #orthopedics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Brudzinski’s Sign ... Brudzinski's sign ... Passive neck flexion causes ... #Meningitis #Clinical ... #Pediatrics #Peds
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... pathophysiology #peds ... #pediatrics
Froment’s Test for Ulnar Nerve Palsy

This tests for pinch grip weakness caused by ulnar nerve palsy,
grip weakness caused ... Froment's Sign is ... Jeanne’s sign is ... #Froments #Sign ... #video #neurology
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 ... Lower #Extremity #tone ... #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
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics