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Blau Syndrome, the prototypic auto-inflammatory granulomatous disease
Blau syndrome is a monogenic disease resulting from mutations in the pattern recognition receptor NOD2, and is phenotypically characterized by the triad of granulomatous polyarthritis, dermatitis and uveitis. This paper reviews briefly the classical clinical features of the disease, as well as more...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4136643/ https://ncbi.nlm.nih.gov/pubmed/25136265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1546-0096-12-33 |
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