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21hydroxylasedeficiency genetics glftap macroadenoma masseffects mnemonic pediatrics peds pituitary sideeffects
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
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
Signs / Symptoms ... / Complications ... • Post-nasal drip ... #SideEffects #endocrinology ... mnemonic #GLFTAP #pathophysiology
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