The Calgary Guide to Understanding Disease @TheCalgaryGuide
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pathophysiology genetics 21hydroxylasedeficiency 21ohd benign bph childhood diagnosis endocrinology immunization praderwilli prostate prostatic signs symptoms syndrome
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Complications: • Gonadal hypoplasia ... pathophysiology #peds ... #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
congenital adrenal hyperplasia ... endocrinology #peds ... #pediatrics
Benign Prostatic Hyperplasia: Pathogenesis and Clinical Findings Hormonal alterations (result of aging process) ->
Benign Prostatic Hyperplasia ... Inflammation: Incr tissue injury ... chronic renal injury ... Benign #Prostatic #Hyperplasia ... Pathophysiology #Urology
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
metabolites induce injury ... #Immunization #peds ... #pediatrics #pathophysiology
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