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21hydroxylasedeficiency 21ohd dengue diagnosis endocrinology fever pathophysiology pediatrics peds severity
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... vomiting • Late (shock ... ): cold & mottled ... pathophysiology #genetics
Modified dengue severity classification, PAHO/WHO Dengue without warning signs - DNWS: • Person who lives or has
dengue severity classification ... include any child coming ... Shock or respiratory ... Shock evidenced ... , tachycardia, cold
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