The Calgary Guide to Understanding Disease @TheCalgaryGuide
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21hydroxylasedeficiency benzodiazepine diagnosis endocrinology genetics peds pharmacology symptoms
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 ... #pathophysiology ... endocrinology #peds #pediatrics
Benzodiazepine (BZD) withdrawal: clinical findings and complications • Activation of ACC and OFC -> Feelings of
Benzodiazepine (BZD ... ) withdrawal: clinical ... findings and complications ... #pathophysiology ... #diagnosis #signs
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