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

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Bevacqua, Martina | Bastard, Paul | Pinhas, Yael | Aubart, Mélodie | Roux, Charles-Joris | Taha, Muhamed-Kheir | Cohen, Jérémie, F

Edité par CCSD ; Lippincott, Williams & Wilkins -

International audience.

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.

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