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21hydroxylasedeficiency clinical diagnosis encephalopathy galant genetics management normal physicalexam posterior pres reflex reversible 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 ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Galant Reflex on Physical Exam The Galant reflex is present at birth and remains until the 2nd
possible change in tone ... persistent in cases ... clinical #video #Neurology ... #Peds #Pediatrics ... #Normal #Primitive
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 Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
may precede the neurologic ... Etiology: • Pathophysiology ... the underlying cause ... Seizures: Treat with AEDs ... until cause identified
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