Mimori dementia signs symptoms algorithm hypokalemia disease 21ohd differential cord genetics peds

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

Signs/Symptoms/Complications ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics ... endocrinology #peds

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