Properdin deficiency, type III

MedGen UID:: 326887
•Concept ID:: C1839456
•: Disease or Syndrome

Synonym:	Properdin Deficiency, Type III

OMIM®:	300383; 312060

Recent clinical studies

Diagnosis

Carrier detection in families with properdin deficiency by microsatellite haplotyping.

Kölble K, Cant AJ, Fay AC, Whaley K, Schlesinger M, Reid KB
J Clin Invest 1993 Jan;91(1):99-102. doi: 10.1172/JCI116207. PMID: 8423238 Free PMC Article

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Prognosis

A properdin dependent nephritic factor slowly activating C3, C5, and C9 in membranoproliferative glomerulonephritis, types I and III.

Clardy CW, Forristal J, Strife CF, West CD
Clin Immunol Immunopathol 1989 Mar;50(3):333-47. doi: 10.1016/0090-1229(89)90141-4. PMID: 2917424

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Properdin deficiency, type III

Recent clinical studies

Diagnosis

Prognosis

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