The Calgary Guide to Understanding Disease @TheCalgaryGuide
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21hydroxylasedeficiency diagnosis endocrinology genetics incontinence pediatrics peds signs symptoms urinary
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 ... endocrinology #peds #pediatrics
Mixed Urinary Incontinence: Pathogenesis and Clinical Findings Urgency Urinary Incontinence (UUI) -> Urinary leakage preceded by a
Mixed Urinary Incontinence ... Incr PVR if a complication ... #Incontinence #Mixed ... #Pathophysiology ... Signs #Symptoms #Urology
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