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diagnosis hematology treatment acromegaly common endocrinology hemophagocytic hypogammaglobulinemia immunodeficiency immunology lymphohistiocytosis pathophysiology variable
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... signs and symptoms ... lymph node, or liver ... Lymphohistiocytosis #diagnosis #management
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to impaired B-cell ... to 8 years Clinical ... disease • Liver ... : • Nephrotic syndrome ... (Epstein-Barr syndrome
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
GrepMed Handbook Clinical ... Mortality due to CVD ... GH stimulates liver ... Beckwith Wiedemann syndrome ... adenoma, ↓(TFT, LH
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