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diagnosis management hematology differential peds kawasaki rheumatology syndrome comparison hemophagocytic hlh lymphohistiocytosis manifestations sclerosis aids algorithm als amyotrophic behcet bells
Manifestations of IgG4-related disease by organ system. The most common primary disease features are indicated in
of IgG4-related disease ... common primary disease ... features are indicated ... Systems #Diagnosis #Hematology ... #Signs #Symptoms
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Kawasaki Disease ... Affects children ... #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
Clinical features of focal cortical brain lesions in a right-handed individual Frontal, either: Intellectual impairment, Personality
Clinical features ... Homonymous field defect ... #Localization #Symptoms ... #Signs #Diagnosis ... #Neurology
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... of Liver Disease ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... #Hepatology
Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
neurodegenerative disease ... Afferent pupillary defect ... SIGNS/SYMPTOMS ... Signs and symptoms ... #treatment #MS
Kawasaki Disease - Timeline of Clinical Features and Complications - Fever >5 days - 4
Kawasaki Disease ... of the 5 other features ... #Kawasaki #Disease ... #Signs #Symptoms ... #Peds #Pediatrics
Clinical Features of Systemic Lupus (SLE) General: Fever (50%), Depression, Fatigue (75%), Weight loss (50%) Eye: Sjögrens (15%) Skin
Clinical Features ... Restrictive lung defect ... pain (20%) Renal disease ... erythematosus #signs ... #symptoms #diagnosis
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
When present, symptoms ... , signs, and complications ... • "Vasomotor" symptoms ... von Willebrand disease ... #hematology
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
most frequently affects ... age, however the disease ... Diagnosis: HLH signs ... and symptoms can ... #hematology
Features of a Sickle Cell Crisis Sickle-cell disease - an autosomal recessive blood disorder. Characterized by red
Features of a Sickle ... Sickle-cell disease ... Sickle cell disease ... almost exclusively affects ... #Signs #Symptoms
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