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differential hematology management treatment gastroenterology abnormal algorithm cirrhosis dermatology hepatopulmonary pathophysiology signs syndrome achalasia acidosis alkaline alp anemia antimda5 antimda5dm
Algorithm regarding the diagnosis and treatment of Hereditary Hemochromatosis HH. Step 1: In the patient with
regarding the diagnosis ... of liver disease ... If other causes ... hemochromatosis #algorithm #diagnosis ... #management #hepatology
Abnormal liver function tests algorithm. This figure details the initial response to abnormal liver blood tests.
Areas of diagnostic ... disease; AST, aspartate ... disease; T2DM, ... Abnormal #Algorithm #Hepatology ... #Differential #Diagnosis
Portal Hypertension - Differential Diagnosis Portal Pressure = the pressure difference between the pressure in the portal
- Differential Diagnosis ... >10 mmHg - clinically ... sarcoidosis) • Liver ... Veno-occlusive disease ... #causes #hepatology
Asterixis is a type of negative myoclonus characterized by irregular lapses of posture of various body
characterized by irregular lapses ... associated with liver ... disease (hepatic ... hyperammonemia #PhysicalExam ... #clinical #diagnosis
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 Hepatopulmonary Syndrome - Diagnosis and Management Summary A defect in arterial oxygenation due to a gas exchange
disease and in ... Caused by intrapulmonary ... shunt (Type 2) Clinical ... Should be performed ... management #treatment #hepatology
Causes of Lactate Elevation, Lactic Acidosis - Differential Diagnosis The most common causes of hyperlactatemia are usually:
- Differential Diagnosis ... of lactate as a clinical ... What we should be ... presentations and disease ... recognized and should
Venous Thrombosis vs Arterial Thrombosis - Differential Diagnosis Framework VENOUS THROMBOSIS • Acquired Risk Factors: - >48 hours
- Differential Diagnosis ... Myeloproliferative disease ... Syndrome, Ischemic Liver ... antibodies (APLS should ... #differential #diagnosis
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
late adulthood • Diagnosis ... to 8 years Clinical ... • Liver diseases ... conditions Diagnosis ... DDX - Other causes
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... age, however the disease ... lymph node, or liver ... • Infection should ... antibiotic therapy should
Bleeding and Bruising - Disorders of Hemostasis - Differential Diagnosis Framework == Quantitative or Qualitative defect in
- Differential Diagnosis ... of factor VII should ... discern these causes ... #Differential #Diagnosis ... #Hematology
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