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