44 results
diagnosis video gowers pathophysiology dystrophy muscular peds management meningitis brudzinskis urology msk shock cardiogenic dmd duchenne genetics 21hydroxylasedeficiency abcdes acute
Brudzinski's Sign on Physical Exam - Meningitis #Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
Brudzinski's Sign ... #Brudzinskis #Sign ... #PhysicalExam # ... clinical #video ... #neurology #peds
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 Cardiogenic Shock: Pathogenesis, complications and clinical findings #Cardiogenic #Shock #pathophysiology #cardiology #diagnosis #signs #symptoms
complications and clinical ... Cardiogenic #Shock #pathophysiology ... #cardiology #diagnosis ... #signs #symptoms
Gowers' Sign on Physical Exam Seen in this patient with Duchenne muscular dystrophy (DMD) #Gowers #Sign #PhysicalExam #neurology
Gowers' Sign on ... DMD) #Gowers #Sign ... #PhysicalExam # ... neurology #clinical ... #video #pediatrics
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 Clinical Examination of the Cardiovascular System #Cardiovascular #PhysicalExam #Diagnosis #Signs #Symptoms #Cardiology
Clinical Examination ... Cardiovascular #PhysicalExam ... #Diagnosis #Signs ... #Symptoms #Cardiology
Brudzinski's sign is a physically demonstrable symptom of meningitis. It is characterized by reflexive flexion of
Brudzinski's sign ... #Brudzinskis #sign ... #clinical #video ... #neurology #meningitis ... #physicalexam
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 Spondylolysis & Spondylolisthesis: Pathogenesis and Clinical Findings Pars interarticularis stress fracture (spondylolysis) - most frequently in the
Pathogenesis and Clinical ... Stork test) • XR ... — scotty dog sign ... MSK #diagnosis #pathophysiology ... #signs #symptoms
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 ... #Pediatrics #Peds ... #neurology
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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 ... , sleep apnea, cor ... Syndrome #genetics #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 ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds #pediatrics
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
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