Stevens-Johnson syndrome (SJS) is an uncommon, severe skin and mucous membrane disease. It is generally due to a drug response that begins with flu-like symptoms and progresses to a painful rash that spreads and blisters. After a few days, the layers on the top of the affected skin die, shed, and begin to regenerate.
Ocular Surface Reconstruction in Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis
Ocular surface reconstruction procedures have shown a significant recovery of vision and the ocular surface in patients with SJS and TEN.
