The Calgary Guide to Understanding Disease @TheCalgaryGuide
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21hydroxylasedeficiency genetics glftap macroadenoma masseffects pediatrics pituitary sideeffects
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
following order; GH ... A good mnemonic ... #SideEffects #endocrinology ... #mnemonic #GLFTAP ... #pathophysiology
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