26 results
diagnosis physicalexam signs video management meningitis pathophysiology normal primitive reflex brudzinskis differential genetics sclerosis spinalcord syndrome timeline treatment 21hydroxylasedeficiency 21ohd
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 #pediatrics
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 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 ... #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds #neurology
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 Brudzinski's sign is a physically demonstrable symptom of meningitis. It is characterized by reflexive flexion of
Brudzinski's sign ... physically demonstrable symptom ... flexion of the knees and ... #clinical #video ... #neurology #meningitis
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 Brudzinski's Sign on Physical Exam - Meningitis via @TheIntern254 #Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics
Brudzinski's Sign ... #Brudzinskis #Sign ... #PhysicalExam #clinical ... #video #neurology ... #peds #pediatrics
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 Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... and Complications ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds ... #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
clinical findings ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... pathophysiology #peds ... #pediatrics
Asymmetrical Tonic Neck Reflex (ATNR) This primitive reflex found in newborn babies that normally vanishes around 4
infant's arms and ... the arm and leg ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
: Pathogenesis and ... Clinical Findings ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
Signs and symptoms ... patients with clinically ... stimulation Clinical ... objective evidence of neurologic ... diagnosis #management #neurology
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