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21hydroxylasedeficiency genetics gout homeostasis medications pediatrics peds uricacid
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Uric Acid Homeostasis In the liver, purines are metabolized to uric acid. The last step in purine
The last step in purine ... Homeostasis #Gout #Pathophysiology ... #Pharmacology # ... Medications #Management
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