Figure 2.

Fitting of scleral lenses in patients with Stevens–Johnson syndrome (SJS) sequelae: (a) Left eye of a patient with SJS sequelae showing corneal vascularisation, stromal scarring in the inferonasal cornea, conjunctivalization inferiorly from 5 to 8 o’clock with a well-centered scleral lens, the two black dots on the lens suggests the left-sided laterality of the scleral lens for easy identification of the lens by the patient. (b) The right eye of a patient with SJS sequelae showing a scleral lens, and total limbal stem cell deficiency with corneal scarring was seen although significant visual improvement was not seen with scleral lenses, the patient’s photophobia was reduced and she was comfortable with the scleral lens. (c) Right eye of a patient with SJS sequelae fitted with a scleral lens post mucous membrane grafting in the upper and lower eyelids