Properdin deficiency: Difference between revisions
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{{Infobox medical condition |
{{Infobox medical condition |
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| Name = Properdin deficiency |
| Name = Properdin deficiency |
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| Image = |
| Image = X-linked recessive.svg |
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| image_size = 140px |
| image_size = 140px |
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| Caption = This condition is inherited in an x-linked recessive manner |
| Caption = This condition is inherited in an x-linked recessive manner |
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Revision as of 06:03, 7 November 2017
| Properdin deficiency |
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Properdin deficiency is a rare X-linked disease in which properdin, an important complement factor, 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.
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