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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Detalles Bibliográficos
Autores principales: Naik, Anmol U, Annamalai, Radha, Biswas, Jyotirmay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Reports
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

Internet

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

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