Familial chilblain lupus due to a novel mutation in TREX1 associated with Aicardi –Goutie’res syndrome

Familial chilblain lupus (FCL) is a rare, chronic form of cutaneous lupus erythematosus, which is characterized by painful bluish-red inflammatory cutaneous lesions in acral locations. Mutations in TREX1, SAMHD1 ...
Source: Pediatric Rheumatology - Category: Rheumatology Authors: Tags: Case Report Source Type: research