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pediatrics 21hydroxylasedeficiency brudzinskis clinical comatose diagnosis endocrinology genetics meningitis neurology video
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 ... non-arousable, decr urine ... #pathophysiology ... endocrinology #peds
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 ... Clinical #Video #PhysicalExam ... #Pediatrics #Peds
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 The Neurological Evaluation of a Comatose Patient Definition: • Coma: a state of unresponsiveness; the absence of
• Mutism Pathophysiology ... • Vestibulo-ocular ... • Examine for signs ... Casey Albin MD @ ... caseyalbin #PhysicalExam
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