| Literature DB >> 31870725 |
Chai Teng Chear1, Revathy Nallusamy2, Scott W Canna3, Kwai Cheng Chan2, Mohd Farid Baharin4, Munirah Hishamshah4, Hamidah Ghani5, Adiratna Mat Ripen4, Saharuddin Bin Mohamad6.
Abstract
Autoinflammatory disorders are characterized by dysregulated innate immune response, resulting in recurrent uncontrolled systemic inflammation and fever. Gain-of-function mutations in NLRC4 have been described to cause a range of autoinflammatory disorders. We report a twelve-year-old Malay girl with recurrent fever, skin erythema, and inflammatory arthritis. Whole exome sequencing and subsequent bidirectional Sanger sequencing identified a heterozygous missense mutation in NLRC4 (NM_001199138: c.1970A > T). This variant was predicted to be damaging in silico, was absent in public and local databases and occurred in a highly conserved residue in the leucine-rich repeat (LRR) domain. Cytokine analysis showed extremely high serum IL-18 and IL-18/CXCL9 ratio, consistent with other NLRC4-MAS patients. In summary, we identified the first patient with a novel de novo heterozygous NLRC4 gene mutation contributing to autoinflammatory disease in Malaysia. Our findings reinforce the likely pathogenicity of specific LRR domain mutations in NLRC4 and expand the clinical spectrum of NLRC4 mutations.Entities:
Keywords: Autoinflammatory disease; Inflammasome; NLRC4; Whole exome sequencing
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Year: 2019 PMID: 31870725 DOI: 10.1016/j.clim.2019.108328
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969