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21hydroxylasedeficiency dengue diagnosis endocrinology fever genetics pathophysiology pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Severity depends ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Modified dengue severity classification, PAHO/WHO Dengue without warning signs - DNWS: • Person who lives or has
Modified dengue severity ... classification, ... Progressive increase ... , tachycardia, cold ... #classification
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