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21hydroxylasedeficiency diagnosis differential genetics hyperthyroidism pathophysiology pediatrics peds signs symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... mutation in CYP21A2 coding ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology
Hyperthyroidism Overview Clinical Manifestation of Hyperthyroidism: • Fatigue • Weight loss • Heat intolerance • Depression, nervousness
Hyperthyroidism Overview Clinical ... Toxicosis • Iodine ... ↑ T3 - Mild hypercalcemia ... hyperthyroidism #causes ... #differential #endocrinology
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