106 results
diagnosis treatment differential rheumatology algorithm clinical hematology neurology ophthalmology dermatology gastroenterology nephrology pharmacology physicalexam video infections slitlamp classification guidelines krukenbergs
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
Behçet's Syndrome ... ulceration • Ocular ... spondyloarthritis • Ocular ... Leukemia, Lymphoma Ocular ... #diagnosis #management
End Stage Liver Disease (Cirrhosis) - Complications • Ascites • Esophageal Varices • Hepatic
End Stage Liver Disease ... Hepatopulmonary Syndrome ... • Hepatorenal Syndrom ... Complications #diagnosis #management
Behcet's Syndrome - Treatment Ulcers: • Treatment: Topical steroids • Prevention: Colchicine • Azathioprine for refractory disease Arthritis:
Behcet's Syndrome ... for refractory disease ... refractory lesions Ocular ... #Syndrome #Treatment ... #management #pharmacology
Behcet's Syndrome - Diagnosis Diagnostic Criteria for Behget's Syndrome (International Study Group for Behget's Disease): • Recurrent,
Behcet's Syndrome ... Criteria for Behget's Syndrome ... Group for Behget's Disease ... disease: Uveitis ... EricsMedicalLectures/ #Behcets #Syndrome
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Adult-Onset Still's Disease ... cancers • Systemic diseases ... autoinflammatory diseases ... • Ocular: uveitis ... #diagnosis #management
Neuromyelitis Optica (NMO) - Clinical Manifestations • Optic neuritis: Reduced visual acuity, ranging from mild to
desaturation, Scotoma, Ocular ... mainly AQP4-lgG disease ... Other brainstem syndromes ... mainly MOG-lgG disease ... (AQP4-lgG disease
Hypocalcemia - Diagnosis and Management PTH Independent (↑ PTH) • LOW VIT D -
Diagnosis and Management ... Activation: Liver disease ... , Kidney Disease ... Formation: Hungy Bone Syndrome ... - DiGeorge Syndrome
Cutaneous Manifestations of Monoclonal Gammopathy • Extravascular lg Deposits: Systemic amyloidosis, Nodular amyloidosis, Macroglobulinoderma, Follicular hyperkeratotic
Systemic amyloidosis, Nodular ... Cold agglutinin disease ... secretion: POEMS syndrome ... , Syndrome Schnitzler ... cutis laxa, TEMPI syndrome
Streptococcal Toxic Shock Syndrome (STSS) Complication of invasive GAS disease characterized by shock & MOF → occurs
Streptococcal Toxic Shock Syndrome ... of invasive GAS disease ... , erythematous macular ... #Toxic #Shock #Syndrome ... STSS #treatment #management
Systemic Lupus Erythematosus - Summary Antinuclear (ANA) - 95% - Initial screening test Anti-dsDNA - 50% • Associated
with more severe disease ... Used to monitor disease ... block • Sjogren syndrome ... polymyositis overlap syndrome ... #rheumatology #management
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