Properdin deficiency
| Properdin deficiency | |
|---|---|
 | |
| This condition is inherited in an x-linked recessive manner |
Properdin deficiency is a rare X-linked disease in which properdin, an important complement factor responsible for the stabilization of the alternative C3 convertase, is deficient.[1] Affected individuals are susceptible to fulminant meningococcal disease.
References[]
- ^ van den Bogaard R, Fijen CA, Schipper MG, de Galan L, Kuijper EJ, Mannens MM (July 2000). "Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies". Eur. J. Hum. Genet. 8 (7): 513–8. doi:10.1038/sj.ejhg.5200496. PMID 10909851.
External links[]
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- Complement deficiency
- Rare diseases
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