C5 deficiency
Classical and alternative complement pathways converge in C5 complement factor, to activate the lytic pathway
- mainly synthesized by hepatocytes, but also by monocytes, lymphocytes and lung, spleen and fetal intestine cells
- C5 gene is located in chromosome 9q34.1
- C5 complement deficiency
- a rare autosomal recessive inherited disease, associated with recurrent infections episodes, particularly meningitis and extragenital gonorrhea by Neisserial species - these are the most frequent micro-organisms isolated in these patients (1)
- explained because sera from C5 deficiency patients lack bactericidal activity and have severely impaired ability to induce chemotaxis (2)
- a rare autosomal recessive inherited disease, associated with recurrent infections episodes, particularly meningitis and extragenital gonorrhea by Neisserial species - these are the most frequent micro-organisms isolated in these patients (1)
Reference:
- Peter et al.Meningoccocal meningitis in familial deficiency of the fifth component of complement. Pediatrics 1981;67: 882–886.
- Wetsel, 2000 Wetsel, R.A., 2000. The complement. In: Morley, B.J., Walport, M.J., (Eds.), Facts Book Series, Academic Press, pp. 104–109.
Related pages
Create an account to add page annotations
Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page