7312 results
Diagnosis of IgA Vasculitis (Henoch-Schönlein Purpura) - French Vasculitis Study Group 

1) Suggestive clinical manifestations
Diagnosis of IgA ... 1) Suggestive clinical ... individuals - Clinical ... Elevated serum IgA ... - Dominant IgA
Comprehensive pathogenesis of IgA Nephropathy (i.e Berger’s Disease). 

IgA Nephropathy is the most common cause of
pathogenesis of IgA ... IgA Nephropathy ... - Why is IgA Nephropathy ... complement to IgA ... BergersDisease #clinical
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings

 - Infectious Agents - 50% have
IgA Vasculitis – ... Pathogenesis and Clinical ... (GD-IgA1). ... -> Decr IgA serum ... -> adhesion of IgA
Antiphospholipid Syndrome (APLS) Testing - Hypercoagulable Workup Algorithm
INDICATIONS FOR TESTING:
 • Vascular thrombosis
- 1 or more clinical ... and IgM • Beta ... Antibodies, IgG ... Cardiolipin Antibody, IgA ... Glycoprotein 1 Antibody, IgA
Palpable Purpura seen in Henoch Schonlein Purpura (HSP, IgA Vasculitis)

55 year old male on tuberculosis treatment
Purpura (HSP, IgA ... Schonlein #HSP #IgA ... #Vasculitis #clinical
Dermatological semiology of Cutaneous Vasculitis 

Clinicopathologic correlations
 • Purpura, papules, pustules, necrosis: involvement of small vessels
: SLE +++ • IgA ... lesions #diagnosis #clinical
X-Linked Agammaglobulinemia: Pathogenesis and clinical findings
The epidemiology of this disease is 1/340,000 births and roughly double
Pathogenesis and clinical ... undetectable levels of IgA ... , IgG, and IgM
Staphylococcus-associated GlomeruloNephritis - Diagnosis and Management Summary
CLINICAL
 • Nephritic syndrome (Casts)
 • Marked proteinuria (may be
Management Summary CLINICAL ... • C3/lgG or IgA
Cryoglobulinemia Classification Types

Type 1: Monoclonal IgM (rarely IgG/lgA)
 • Raynaud phenomenon, Digital ulcers/gangrene, Livedo reticularis, Hyperviscosity
1: Monoclonal IgM ... (rarely IgG/lgA ... 2: Monoclonal IgM ... and polyclonal IgG ... and polyclonal IgG
Common Variable Immunodeficiency (CVID)

What?
CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... : • Low serum IgG ... ) • Low serum IgA ... and/or IgM, age ... trough levels of IgG