The Calgary Guide to Understanding Disease @TheCalgaryGuide
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pathophysiology 21hydroxylasedeficiency bzd diagnosis endocrinology genetics pediatrics withdrawal
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Benzodiazepine (BZD) withdrawal: clinical findings and complications • Activation of ACC and OFC -> Feelings of
Benzodiazepine ( ... sudden death #Benzodiazepine ... BZD #withdrawal #pharmacology ... pathophysiology #diagnosis #signs ... #symptoms
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