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diagnosis differential management beriberi cellulitis deficiency disease hematology histiocytosis hypertension idsa infections korsakoff langerhans lch manifestations nutrition pathophysiology phtn pulmonary
Clinical Classification of Pulmonary Hypertension 1. Pulmonary arterial hypertension from pulmonary vasculopathy Idiopathic pulmonary arterial hypertension Heritable gene mutations
Clinical Classification ... protein receptor type ... activin A receptor type ... pulmonary Langerhans cell ... #Differential #Causes
IDSA Algorithm for the Management of Purulent skin and soft tissue infections (SSTIs). Mild infection: for
IDSA Algorithm for ... Moderate infection ... or those with clinical ... evidence of organ dysfunction ... including those caused
Von Willebrand Disease Classification Type 1 (Accounts for ~3/4 of cases): • Defect: Quantitative defect (i.e. not
Willebrand Disease Classification ... Qualitative defect (i.e. dysfunctional ... • Bleeding: Moderate-severe ... Bleeding: Severe (Clinically ... VonWillebrand #Disease #Classification
Thiamine Deficiency - Differential Diagnosis Framework and Clinical Manifestations Causes of Thiamine Deficiency: • Poor intake: - Diets
Framework and Clinical ... Manifestations Causes ... rice/processed grains ... and myocardial dysfunction ... triggers Right HF • Moderate
Langerhans Cell Histiocytosis (LCH) Granulomatous Lesions comprising langerin-positive histiocytes and an inflammatory infiltrate can arise in virtually
, a type of dendritic ... various tissues, leading ... populations) CLINICAL ... • Endocrine Dysfunction ... marrow: Organ dysfunction
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