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21hydroxylasedeficiency acute endocrinology genetics glaucoma pediatrics peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
Acute Closed Angle Glaucoma: Pathogenesis and Clinical Findings OPHTHALMIC EMERGENCY: Early detection is essential, but most patients
lights are a key symptom ... / Complications ... Photophobia #Acute #ClosedAngle ... #Glaucoma #pathophysiology ... #ophthalmology
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