Severe Meningococcal Meningitis Revealing a Novel Form of Properdin Deficiency in a Previously Healthy 13-Year-old Child

Pediatr Infect Dis J. 2024 Aug 1;43(8):e282-e284. doi: 10.1097/INF.0000000000004397. Epub 2024 May 10.

Abstract

A 13-year-old boy was admitted with severe meningococcal meningitis. Immunologic workup revealed a properdin deficiency, and genetic sequencing of CFP identified a novel, private and predicted pathogenic variant in exon 8. The patient received broad immunizations and penicillin prophylaxis. Children with invasive meningococcal disease should be tested for complement deficiency.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Humans
  • Male
  • Meningitis, Meningococcal* / diagnosis
  • Neisseria meningitidis / genetics
  • Properdin* / deficiency
  • Properdin* / genetics

Substances

  • Properdin