Hyper IgM syndrome and complement Clq deficiency in an individual with systemic lupus erythematosus-like disease

Clin Exp Rheumatol. 2010 Jul-Aug;28(4):558-60. Epub 2010 Aug 30.

Abstract

Many immunedeficiency syndromes are associated with autoimmune disorders. We here report on a girl with a systemic lupus erythematosus-like disease who suffered from both hyperimmunoglobulin M syndrome (HIGMS) and C1q deficiency. Despite severe central nervous system-lupus like disease, probably due to C1q deficiency, kidney function was relatively spared. IgM autoantibody might play a protective role against lupus-glomerulonephritis.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Complement C1q / deficiency*
  • Female
  • Humans
  • Hyper-IgM Immunodeficiency Syndrome / complications*
  • Hyper-IgM Immunodeficiency Syndrome / diagnosis
  • Immunoglobulin M / physiology
  • Lupus Erythematosus, Systemic / complications
  • Lupus Erythematosus, Systemic / diagnosis
  • Lupus Erythematosus, Systemic / etiology*
  • Lupus Nephritis / physiopathology
  • Lupus Nephritis / prevention & control

Substances

  • Immunoglobulin M
  • Complement C1q