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Letter to the Editor

Type 1 Boston Keratoprosthesis for Limbal Stem Cell Deficiency in Epidermolysis Bullosa

, BS Opt ORCID Icon, , MBBS, MTech, PhD ORCID Icon & , MBBS, MS ORCID Icon

References

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  • Aravena C, Bozkurt TK, Yu F, et al. Long-term outcomes of the boston type I keratoprosthesis in the management of corneal limbal stem cell deficiency. Cornea. 2016;35:1156–1164.
  • Vazirani J, Mariappan I, Ramamurthy S, et al. Surgical management of bilateral limbal stem cell deficiency. Ocul Surf. 2016;14:350–364.
  • Thanos M, Pauklin M, Steuhl KP, et al. Ocular surface reconstruction with cultivated limbal epithelium in a patient with unilateral stem cell deficiency caused by Epidermolysis bullosa dystrophic hallopeau-Siemens. Cornea. 2010;29:462–464.
  • Sejpal K, Ali MH, Maddileti S, et al. Cultivated limbal epithelial transplantation in children with ocular surface burns. JAMA Ophthalmol. 2013;131:731–736.
  • Brown C, Rowlands M, Lee D, et al. Keratoprosthesis in pediatric keratitis-icthyosiform-deafness syndrome. J Aapos. 2016;20:73–75.
  • Basu S, Taneja M, Narayanan R, et al. Short-term outcome of Boston Type 1 keratoprosthesis for bilateral limbal stem cell deficiency. Indian J Ophthalmol. 2012;60:151–153.
  • Ahmad S, Mathews PM, Srikumaran D, et al. Outcomes of repeat Boston type 1 keratoprosthesis implantation. Am J Ophthalmol. 2016;161:181–187.e181.
  • Fung SSM, Jabbour S, Harissi-Dagher M, et al. Visual outcomes and complications of type I Boston keratoprosthesis in children: a retrospective multicenter study and literature review. Ophthalmology. 2017. doi:10.1016/j.ophtha.2017.07.009.

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