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diagnosis management rheumatology differential oncology hepatology pathophysiology syndrome algorithm dermatology arthritis clinical complications neurology workup anemia causes disease gammopathy monoclonal
Symptoms of Hypophosphatemia • CNS: Seizures, Delirium, Paresthesias, Central & extrapontine myelinolysis, Hallucinations, Fatigue • Hematologic:
Symptoms of Hypophosphatemia ... Hallucinations, Fatigue • Hematologic ... Heart failure • Bones ... Growth retardation, Bone ... #Signs #Diagnosis
Eosinophil Disorders Testing Algorithm INDICATIONS FOR TESTING: • Peripheral blood eosinophilia/hypereosinophilia uncovered incidentally during medical evaluation or
Eosinophil Disorders ... glucocorticoid treatment ... organ-specific signs ... or symptoms (eg ... Differential #diagnosis #hematology
Aplastic Anemia - Illness Script Signs and symptoms: • Recurrent infections from neutropenia • Mucosal bleeding from
Illness Script Signs ... and symptoms: ... with hypocellular bone ... megaloblastic anemia Treatment ... #hematology
Post-Transplantation Lymphoproliferative Disorders (PTLD) Definition: Lymphoid and/or plasmacytic proliferations that occur as a result of immunosuppression in
Lymphoproliferative Disorders ... Conditioning regimen Signs ... , unexplained hematologic ... EBV viral load, signs ... Diagnosis and classification
Lymphomas and Lymphoproliferative Disorders - Differential Diagnosis Algorithm Hodgkin Lymphoma ~40% - Characteristic For Reed-Sternberg (RS) Cells
Lymphoproliferative Disorders ... pattern of spread, B symptoms ... Responsive to Treatment ... #Classification ... pathophysiology #Hematology
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
Hypercellular bone ... When present, symptoms ... , signs, and complications ... • "Vasomotor" symptoms ... #hematology
Causes of Thrombocytopenia and Platelet Disorders - Differential Diagnosis and Workup History: - Prior platelet count, family
pylori test (GI symptoms ... candidate) - Bone ... or if a primary hematologic ... disorder is suspected ... Causes #Workup #hematology
Gaucher Disease Pathophsiology • Lysosomal storage disorder • Deficiency of ß-glucocerebrosidase • Accumulation of glucosylceramide in macrophages Diagnosis
Lysosomal storage disorder ... Osteonecrosis, bone ... Disease #Diagnosis #Signs ... #Symptoms
Clinical Classification of Pulmonary Hypertension 1. Pulmonary arterial hypertension from pulmonary vasculopathy Idiopathic pulmonary arterial hypertension Heritable gene mutations
Clinical Classification ... mutations - BMPR2 (bone ... multifactorial mechanisms Hematologic ... Systemic disorders ... Hypertension #PHTN #Classification
In order to better classify heart failure, the American College of Cardiology Foundation and the American
based solely on symptoms ... With treatment, ... who never show symptoms ... or signs of heart ... past or current symptoms
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