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