The Calgary Guide to Understanding Disease @TheCalgaryGuide
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pathophysiology benign bph diagnosis endocrinology genetics pediatrics peds prostate prostatic signs
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
congenital adrenal hyperplasia ... Signs/Symptoms/Complications ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology
Benign Prostatic Hyperplasia: Pathogenesis and Clinical Findings Hormonal alterations (result of aging process) ->
Benign Prostatic Hyperplasia ... emptying - Voiding Symptoms ... Benign #Prostatic #Hyperplasia ... Pathophysiology #Urology ... #Signs #Symptoms
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