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

• Main Authors: Kelly M. Garrity (Author), Richard Chiu (Author), Rachana Srivastava (Author), Deborah K. McCurdy (Author), Jonathan E. Zuckerman (Author)
• Formato: Livro
• Publicado em: Elsevier, 2024-03-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

Blau syndrome is a rare, autosomal dominant or de novo mutation, granulomatous, auto-inflammatory disorder classically manifesting as a triad of polyarthritis, uveitis, and dermatitis. Rarely, this disease involves visceral sites such as the liver, lung, and kidney. In this report, we describe a cas...