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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...
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| Vydáno v: | Indian J Ophthalmol |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medknow Publications & Media Pvt Ltd
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6173012/ https://ncbi.nlm.nih.gov/pubmed/30249847 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijo.IJO_629_18 |
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