16 results
video orthopedics test hand nerve signs wrist diagnosis fasciitis foot froments genetics neurology newborn pathophysiology plantar podiatry tone windlass 21hydroxylasedeficiency
Froment’s Test for Ulnar Nerve Palsy This tests for pinch grip weakness caused by ulnar nerve palsy,
Froment’s Test for Ulnar ... #Palsy #clinical ... video #neurology #physicalexam ... #msk #orthopedics ... #sports #hand
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 Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... Koplik's spots: ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Ulnar Fovea Sign Test for Fovea Disruption Useful for patients with pain along the ulnar aspect of
Ulnar Fovea Sign ... #wrist #clinical ... #video #physicalexam ... #orthopedics #msk ... #sports
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 Wartenberg Sign in Ulnar Neuropathy Abnormal abductor the fifth finger due to ulnar neuropathy ( weakness of
Wartenberg Sign ... pinky #finger #clinical ... #video #physicalexam ... #neurology #msk ... #sports #orthopedics
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 Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... Extremities #PhysicalExam ... #Signs #Symptoms ... #Dehydration #Peds ... #Pediatrics
Froment's Sign - Ulnar Nerve Injury Patients with compromise of the ulnar nerve will not be able
Froment's Sign - ... Ulnar Nerve Injury ... Injury #Hand #PhysicalExam ... #clinical #video ... #sports #msk #orthopedics
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 Tinel's Test of the Ulnar Nerve Perform a Tinel's at the cubital tunnel by percussing the ulnar
Tinel's Test of the Ulnar ... #Tinels #Test #Sign ... elbow #PhysicalExam ... #clinical #video ... #sports #msk #orthopedics
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 Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... fractures • Short ... pathophysiology #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 ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... Findings #Diagnosis #Peds ... #Pediatrics #Hepatology
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