The Calgary Guide to Understanding Disease @TheCalgaryGuide
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21hydroxylasedeficiency complications diagnosis genetics hypertensive pediatrics peds retinopathy symptoms
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
Chronic Hypertensive Retinopathy: Pathogenesis and clinical findings Ophthalmic Artery Hypertension Stage 1: Mild/vasoconstrictive • Acute and chronic vasospasm
Chronic Hypertensive ... • Acute and chronic ... #Retinopathy #pathophysiology ... #ophthalmology ... #diagnosis #signs
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