2 results
21hydroxylasedeficiency endocrinology glaucoma ophthalmology pediatrics peds secondary
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 ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Primary Open-Angle Glaucoma: Pathogenesis and Clinical Findings • Risk factors -> Incr IOP, Incr age, African-American
Pathogenesis and Clinical ... vascular disease • Genetic ... myocilin, OPTN gene encoding ... #Secondary #OpenAngle ... #Glaucoma #pathophysiology
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