Create issue ticket

256 Possible Causes for Hypocomplementemia

  • Systemic Lupus Erythematosus

    Since she had arthritis, lymphopenia, hypocomplementemia, and anti-nuclear and anti-double-stranded DNA antibodies, she was diagnosed with systemic lupus erythematosus (SLE[] She also had concomitant massive hematuria and proteinuria, fever, multiple positive autoimmune antibodies, hypocomplementemia, abnormal lumbar puncture findings and evidence[] Laboratory findings on admission revealed proteinuria, microscopic hematuria, anemia, leukopenia, hypoalbuminemia, hypocomplementemia, and slightly elevated levels of serum[]

  • Hypocomplementemic Vasculitis

    His disease resembled the hypocomplementemic vasculitis syndrome but was atypical in its early age of presentation, severe hypocomplementemia, and progression to end-stage[] In 1995, after complete remission, he developed nephrotic syndrome with chronic urticaria and hypocomplementemia.[] Overview A rare condition characterized by the presence of recurring urticarial vasculitis, arthralgia or arthritis and hypocomplementemia.[]

  • Complement Deficiency Syndrome

    Workup often shows hypocomplementemia ( C3/C4), renal failure, eosinophilia and eosinophiluria.[] Circulating enzyme deficiency Complement 4 deficiency Complement deficiency c4 Complement deficiency disease Deficiency of circulating enzyme Hereditary angioneurotic edema Hypocomplementemia[] Hypocomplementemia is a frequent but nonspecific marker of GN in bacterial endocarditis.[]

  • Complement 3 Deficiency

    Acquired hypocomplementemia may occur in the setting of bone infections (osteomyelitis), infection of the lining of the heart (endocarditis), and cryoglobulinemia.[] Immune complex disease C1q deficiency – SLE, recurrent infections C1r deficiency and C1s deficiency – SLE with prominent renal and cutaneous disease Anti-C1q antibodies Hypocomplementemia[] Circulating enzyme deficiency Complement 4 deficiency Complement deficiency c4 Complement deficiency disease Deficiency of circulating enzyme Hereditary angioneurotic edema Hypocomplementemia[]

  • Membranoproliferative Glomerulonephritis

    In contrast to MPGN type III, the hypocomplementemia in MPGN type I is thought to be, for the most part, the result of classical pathway activation, which is not associated[] A 24-year-old postpartum woman developed nephrotic syndrome and hypocomplementemia.[] Hypocomplementemia in MPGN Hypocomplementemia is a characteristic finding with all types of membranoproliferative glomerulonephritis (MPGN).[]

  • Urticarial Vasculitis

    Joint manifestations occur mainly in cases with hypocomplementemia.[] Response to treatment is variable, and hypocomplementemia and extracutaneous symptoms may indicate the presence of associated systemic disease.[] Hypocomplementemia, negative immune profile and evidence of vasculitis on skin biopsy suggested a diagnosis of hypocomplementemic urticarial vasculitis.[]

  • Heavy Chain Deposition Disease

    The authors also discuss here the relationship of HCDD to hypocomplementemia.[] Fragmented gamma-heavy chains may also induce hypocomplementemia by the activation of the complement pathway.[] We report four γ1-HCDD patients presenting with cutis laxa, hypocomplementemia and hypoalbuminemia.[]

  • Immunotactoid Glomerulopathy

    […] remission of proteinuria and normalization of hypocomplementemia.[] Clinically the patient was diagnosed as having severe nephrotic syndrome, hypocomplementemia, and IgM kappa monoclonal gammopathy.[] We report the case of a patient with immunotactoid glomerulopathy and hypocomplementemia (low C3 level) who developed several episodes of leucocytoclastic skin vasculitis[]

  • Acute Glomerulonephritis

    Five patients (26%) had prolonged hypocomplementemia.[] The role of sialidase in complement activation and in development of hypocomplementemia in patients with postinfectious acute glomerulonephritis (AGN) was investigated.[] Finally, he visited a regional hospital, and hypocomplementemia was noted there.[]

  • IgG4-Related Kidney Disease

    A 25-year-old woman presented with fever, arthralgia and proteinuria exhibiting leukopenia, hypocomplementemia, increased serum IgG and IgG4, and positive antinuclear and[] RESULTS: Hypocomplementemia, positive anti-nuclear antibodies and eosinophilia were confirmed in more than half of the cases.[] […] follows. (1) Presence of some kidney damage, as manifested by abnormal urinalysis or urine marker(s) and/or decreased kidney function with either elevated serum IgG level, hypocomplementemia[]

Further symptoms