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21hydroxylasedeficiency diagnosis hematology hemeonc hemophagocytic hlh lymphohistiocytosis management pediatrics peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... or triggers) is crucial ... Familial) HLH: - Genetic ... Common Signs and Symptoms ... Pathophysiology
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