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Fig. 1 | Pediatric Rheumatology

Fig. 1

From: Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation

Fig. 1

Clinical findings of the patients. a Livedo reticularis of patient 1. b, c, d Erythematous skin lesions of patient 2, which appear as discoid plaques or annular papules. e T2-weighted magnetic resonance image of the brain of patient 2 showing a recent ischemic lesion in the right thalamus and an older lesion in the left thalamus. f Blue finger syndrome due to vascular occlusion in patient 2

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Pediatric Rheumatology

ISSN: 1546-0096