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. Author manuscript; available in PMC: 2020 Oct 24.
Published in final edited form as: J Pediatr Ophthalmol Strabismus. 2015 Aug 19;52 ONLINE:e41–e44. doi: 10.3928/01913913-20150811-01

Figure 1.

Figure 1.

(A) Clinical appearance of a patient with atypical Stevens–Johnson syndrome during the acute phase, after symblepharon lysis and immediately before bilateral amniotic membrane transplantation on day 3 of the hospital course. Symblepharons are not pictured. (B) The right superior and inferior fornices immediately after bilateral amniotic membrane transplantation. (C) The patient 6 weeks after amniotic membrane transplantation with bilateral white and quiet eyes. Symblepharon rings are still in place.