16 results
physicalexam clinical diagnosis management symptoms meningitis ulnar 21hydroxylasedeficiency 21ohd abcde abcs abnormal adhesivecapsulitis apgar assessment breathing brudzinskis comatose cpap differential
Kernig's Sign in Meningitis Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... Meningitis Kernig's sign ... Prakash #Kernigs #Sign ... #PhysicalExam #Pediatrics ... #Peds #neurology
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 Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Passive neck flexion causes ... While the pathophysiology ... #PhysicalExam #Pediatrics ... #Peds
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 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
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 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 ... #sports #hand
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 Newborn Assessment - APGAR Score Assessment of newborn vital signs following labor via a 10-point scale evaluated
newborn vital signs ... via a 10-point scale ... develop long-term neurologic ... #Diagnosis #Peds ... #Pediatrics #APGAR
Hoffman's sign. Even in this specific case, accompanied by a clonus outline (rhythmic contractions). The median
Hoffman's sign. ... patient to relax the hand ... #Hoffmanns #Sign ... Abnormal #clinical #video ... #neurology #PhysicalExam
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 Wartenberg's Sign on Physical Exam Wartenberg's sign consists of involuntary abduction of the little finger, caused by
Wartenberg's Sign ... Wartenberg's sign ... Often a sign of ... #Wartenbergs #Sign ... #hand #mask #ulnar
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 Trendelenburg Gait: Pathogenesis and clinical findings Skeletal Pathology of the Hip • Arthritis • Congenital hip dysplasia
Chondrodysplasia Neurologic ... Trendelenburg #Gait #pathophysiology ... #causes #symptoms ... #signs #diagnosis ... #msk
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
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
test - Cogan sign ... - Peek sign ... immunologic assay - MuSK ... immunosuppressants - Meds ... diagnosis #management #neurology
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