Properdin deficiency, X-linked

A rare, hereditary, primary immunodeficiency due to a complement cascade protein anomaly characterized by significantly increased susceptibility to Neisseria species infections. It only affects males, typically presenting with severe or fulminant meningococcal disease.

Also known as: properdin deficiency, X-linked, properdin deficiency, X-linked, X-linked recessive, CFPD, PFD, complement Factor properdin deficiency, properdin P Factor deficiency, properdin deficiency, type 1, properdin deficiency, type 2

41 clinical trials for this condition and its sub-types, 0 tagged with Properdin deficiency, X-linked itself.