Abstract
Severe coccidioidomycosis is rare, and specific genetic susceptibility to the disease remains unidentified. We describe a patient with disseminated recalcitrant coccidioidomycosis with autosomal dominant interferon-γ receptor 1 deficiency caused by a heterozygous IFNGR1 818del4 mutation. Therefore, the interleukin-12/interferon-γ axis appears to be critical for control of coccidioidomycosis.
Original language | English (US) |
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Pages (from-to) | e62-e65 |
Journal | Clinical Infectious Diseases |
Volume | 49 |
Issue number | 6 |
DOIs | |
State | Published - Sep 15 2009 |
ASJC Scopus subject areas
- Microbiology (medical)
- Infectious Diseases