Blau syndrome

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Blau syndrome is an autosomal dominant disease which characteristically results in a granulomatous rash, arthritis, and uveitis. Blau syndrome was first described in 1985 in two separate reports. Although the description by Jabs and colleagues appeared first, the eponym, Blau, is widely applied to this syndrome. Many prefer the term, pediatric granulomatous arthritis and uveitis to the name, Blau [15].

Original languageEnglish (US)
Title of host publicationIntraocular Inflammation
PublisherSpringer Berlin Heidelberg
Pages881-883
Number of pages3
ISBN (Print)9783540753872, 9783540753858
DOIs
StatePublished - Jan 1 2016

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ASJC Scopus subject areas

  • Medicine(all)

Cite this

Rosenbaum, J. J., Rosenzweig, H., & Martin, T. (2016). Blau syndrome. In Intraocular Inflammation (pp. 881-883). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-540-75387-2_77