Complement deficiency states

Medicine (Baltimore). 1978 Jan;57(1):1-23. doi: 10.1097/00005792-197801000-00001.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Complement C1 / deficiency
  • Complement C1 / genetics
  • Complement C1 Inactivator Proteins / deficiency
  • Complement C2 / deficiency
  • Complement C2 / genetics
  • Complement C3 / deficiency
  • Complement C4 / deficiency
  • Complement C5 / deficiency
  • Complement C6 / deficiency
  • Complement C7 / deficiency
  • Complement C8 / deficiency
  • Complement System Proteins / deficiency*
  • Complement System Proteins / physiology
  • Female
  • Glomerulonephritis / complications
  • Heterozygote
  • Homozygote
  • Humans
  • Infant
  • Lupus Erythematosus, Systemic / complications
  • Male
  • Middle Aged

Substances

  • Complement C1
  • Complement C1 Inactivator Proteins
  • Complement C2
  • Complement C3
  • Complement C4
  • Complement C5
  • Complement C6
  • Complement C7
  • Complement C8
  • Complement System Proteins