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management hematology peds symptoms algorithm disease dermatology differential erythematosus hemophagocytic hlh lupus lymphohistiocytosis neurology sle systemic timeline activation antinxp2 antinxp2dm
Pediatric Inflammatory Multisystem Syndrome Temporally associated with SARS-CoV-2 infection (PIMS-TS) Clinical features all: fever > 101.3 F most: oxygen
Pediatric Inflammatory ... infection (PIMS-TS) Clinical ... features all: ... #coronavirus #diagnosis ... #Signs #Symptoms
Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... Koplik's spots: ... #Measles #Diagnosis ... KoplikSpots #Peds #Pediatrics ... #Timeline #Signs
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Signs/Symptoms ... Incr Skeletal fractures ... • Short stature ... pathophysiology #peds #pediatrics
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis ... Rickets Dysmorphic Features ... Panhypopituitarism Treatment ... #Differential #Diagnosis ... endocrinology #causes #pediatrics
Leukostasis vs Tumor Lysis Syndrome Leukostasis: • Pathophysiology: Large, immature blasts and high WBC count cause hyperviscosity
WBC >100k, + lab signs ... organ damage • Treatment ... worrisome EKG features ... #TLS #diagnosis ... #management #hematology
Clinical Features of Systemic Lupus (SLE) General: Fever (50%), Depression, Fatigue (75%), Weight loss (50%) Eye: Sjögrens (15%) Skin
Clinical Features ... Demyelinating syndromes ... erythematosus #signs ... #symptoms #diagnosis ... #rheumatology
Guillain-Barre Syndrome - Summary Acute AIDP that presents with rapidly progressive flaccid weakness Epidemiology: • 1-2 cases/100,000 per
Guillain-Barre Clinical ... : Starts in legs ... Guillain-Barre Diagnosis ... #diagnosis #management ... #treatment #neurology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Clinical Presentation ... Fever is the main clinical ... Treatment: • Corticosteroids ... #Diagnosis #Management ... #Hematology #Rheumatology
Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
• Or brainstem syndromes ... patients with clinically ... stimulation Clinical ... Multiple Sclerosis Treatment ... taper 3-7 days - Short
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... : HLH signs and ... • Bicytopenia Treatment ... #hematology
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