Properdin deficiency

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Properdin deficiency

Properdin deficiency is 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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version March 2024

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Properdin deficiency?

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Clinical Trials

For a list of clinical trials in this disease area, please click here.