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Uveitis in sporadic Blau syndrome: Long-term follow-up of a refractory case treated successfully with adalimumab
The classic entity of autosomal dominant Blau syndrome (BS) consists of arthritis, dermatitis, and uveitis, occurring as a result of mutations in the NOD2 gene pattern recognition receptor. Sporadic cases are those in which no known gene mutation is identifiable. Uveitis in BS can be refractory to c...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173012/ https://www.ncbi.nlm.nih.gov/pubmed/30249847 http://dx.doi.org/10.4103/ijo.IJO_629_18 |