SLE-like and sicca symptoms in late component (C9) complement deficiency

Ann Rheum Dis. 1987 Feb;46(2):153-5. doi: 10.1136/ard.46.2.153.

Abstract

Hereditary deficiencies in early and late complement components are well known to predispose to SLE-like syndromes or recurrent infection. Hitherto reported C9 deficient cases have usually been healthy subjects, however, and it is not considered that C9 deficiency is associated with any specific disease. We describe a completely C9 deficient patient with possible Sjögren's syndrome and discuss the relationship.

Publication types

  • Case Reports

MeSH terms

  • Autoimmune Diseases / complications*
  • Autoimmune Diseases / genetics
  • Complement C9 / deficiency*
  • Female
  • Humans
  • Middle Aged
  • Pedigree
  • Sjogren's Syndrome / etiology

Substances

  • Complement C9