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Original Articles

Clinical Profile in Genetically Proven Blau Syndrome: A Case Series from South India

, DO, MRCOphth (Lon), MAMS & , MD
Pages 250-256 | Received 28 Nov 2019, Accepted 19 Mar 2020, Published online: 15 Apr 2020

References

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  • Jindal AK, Pilania RK, Suri D, et al. A young female with early onset arthritis, uveitis, hepatic, and renal granulomas: a clinical tryst with Blau syndrome over 20 years and case-based review. Rheumatol Int. May 6 2019. doi:10.1007/s00296-019-04316-6.
  • Naik AU, Annamalai R, Biswas J. Uveitis in sporadic Blau syndrome: long- term follow-up of a refractory case treated successfully with adalimumab. Indian J Ophthalmol. 2018;66(10):1483–1485. doi:10.4103/ijo.IJO_629_18.
  • Jain L, Gupta N, Reddy MM, et al. A novel mutation in helical domain 2 of NOD2 in sporadic Blau syndrome. Ocul Immunol Inflamm. 2018;26(2):292–294. doi:10.1080/09273948.2016.1207789.
  • Janarthanan M, Poddar C, Sudharshan S, Seabra L, Crow YJ. Familial Blau syndrome: first molecularly confirmed report from India. Indian J Ophthalmol. 2019;67(1):165–167. doi:10.4103/ijo.IJO_671_18.

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