Juvenile arthritis caused by a novel FAMIN (LACC1) mutation in two children with systemic and extended oligoarticular course. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Kallinich, Tilmann; Thorwarth, Anne; von Stuckrad, Sae-Lim; Rösen-Wolff, Angela; Luksch, Hella; Hundsdoerfer, Patrick; Minden, Kirsten; Krawitz, Peter
• Is Part Of: Pediatric rheumatology online journal. Volume 14:Issue 1(2016)
• Page Start: 1
• Page End: 4
• Publication Date: 2016-12
• Subjects: Systemic juvenile idiopathic arthritis -- Exome sequencing, FAMIN, LACC1; Pediatric rheumatology -- Periodicals; Rheumatism in children -- Periodicals; 618.92723
• DOI: 10.1186/s12969-016-0124-2
• Languages: English
• ISSNs: 1546-0096

Abstract

Abstract Background The pathophysiological origin of juvenile idiopathic arthritis (JIA) is largely unknown. However, individuals with presumably pathogenic mutations inFAMIN have been reported, associating this gene with a rare subtype of this disorder.FAMIN, that is formerly also referred to asLACC1 orC13orf31, has recently been shown to play a crucial role in immune-metabolic functions and is involved in regulation of inflammasome activation and promotion of ROS production. Case presentation We describe two siblings with severe familial forms of juvenile arthritis in which whole-exome-sequencing revealed a novel homozygous frameshift mutation (NM_153218.2:c.827delC¸. p.(T276fs*2) inFAMIN . Conclusions The observation of a new deleterious mutation adds further evidence that pathogenic mutations inFAMIN are causal for a monogenic form of JIA. Furthermore the associated phenotype is not restricted to systemic JIA, but can also be found in other forms of familial juvenile arthritis.