Blau Syndrome: A Systemic Granulomatous Disease of Cutaneous Onset and Phenotypic Complexity
Author:
Affiliation:
1. Department of Pediatrics; Thomas Jefferson University; Wilmington Delaware
2. Division of Rheumatology; Alfred I. duPont Hospital for Children; Wilmington Delaware
Funder
GlaxoSmithKline
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/pde.13021/fullpdf
Reference22 articles.
1. Familial granulomatous arthritis, iritis, and rash;Blau;J Pediatr,1985
2. Familial granulomatous synovitis, uveitis, and cranial neuropathies;Jabs;Am J Med,1985
3. CARD15 mutations in Blau syndrome;Miceli-Richard;Nat Genet,2001
4. Presence of a sporadic case of systemic granulomatosis syndrome with a CARD15 mutation;Kanazawa;J Investig Dermatol,2004
5. Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis;Rose;J Rheumatol,2005
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