Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members

Results The index case was a 10 year old Afro-Caribbean boy who initially presented with a non-progressive developmental delay and severe chilblains (the chilblains improved with methotrexate). He developed transient acute ataxia and flattened affect, with visual and auditory hallucinations. Parotid swelling, arthritis and proximal myopathy were noted, but autoantibodies were negative and complement studies normal. No viruses were detected in CSF or saliva. EEG was consistent with encephalopathy. Cerebral MRI was normal but basal ganglia calcification was seen on CT. Skin histology was consistent with FCL. His mother and 2 siblings (3 year old brother and 6 year old sister) also had chilblains (each child had a different father). No other family member had developmental delay, other evidence of autoimmunity or inherited metabolic disease. Neither sibling had CT evidence of basal ganglia calcification. All 4 affected family members had heterozygote mutation of the TREX1 gene (p.Asp18Asn).