Blau syndrome complicated by granulomatous tubulointerstitial nephritis and immune complex mediated glomerulonephritis: A case report and review of the literature

Author:

Garrity Kelly M.ORCID,Chiu Richard,Srivastava Rachana,McCurdy Deborah K.,Zuckerman Jonathan E.

Publisher

Elsevier BV

Reference24 articles.

1. Blau Syndrome: NOD2-related systemic autoinflammatory granulomatosis;Takada;G Ital Dermatol E Venereol Organo Uff Soc Ital Dermatol E Sifilogr.,2020

2. Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the NOD2 mutation;Matsuda;Ann Rheum Dis.,2020

3. A young female with early onset arthritis, uveitis, hepatic, and renal granulomas: a clinical tryst with Blau syndrome over 20 years and case-based review;Jindal;Rheumatol Int.,2021

4. Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions;Ting;J Pediatr.,1998

5. Granulomatous nephritis associated with R334Q mutation in NOD2;Meiorin;J Rheumatol.,2007

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