The Calgary Guide to Understanding Disease @TheCalgaryGuide
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pediatrics 21hydroxylasedeficiency 21ohd genetics prematurity retinopathy
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
Retinopathy of Prematurity: Pathogenesis and clinical findings Increased metabolic demand of growing eye -> Excessive VEGF production ->
#Prematurity #peds ... #pediatrics #pathophysiology ... #ophthalmology
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