Stevens-Johnson syndrome (SJS) is a rare but life-threatening medical condition that can cause several ocular complications. The condition can affect people of any age, but it is most commonly ...

After 10 years without sight, Gail Lane, a 75-year-old woman from Victoria, B.C., has regained her vision. She can now see ...

Steven Johnson Syndrome and Toxic Epidermal Necrolysis in a burn unit: A 15-year experience. Burns: Journal of the International Society for Burn Injuries, 43 (1), 200–205. doi: 10.1016/j.burns ...

J Oral Maxillofac Surg 51: 264-268, 1993. Cheriyan S, Patterson R, Greenberger PA, et al: The outcome of Stevens-Johnson syndrome treated with corticosteroids. Allergy Proc 16: 151-155, 1995.

We describe a patient with Stevens-Johnson syndrome (erythema multiforme major) associated with an increase in glipizide dosage administration. Glipizide is a second-generation sulfonylurea ...

More than one-quarter of Stevens-Johnson syndrome and toxic epidermal necrolysis cases worldwide were attributed to antibiotic use, according to a study.“Antibiotics are a well-described cause ...

Stevens-Johnson syndrome (SJS) is the rare disorder that gave Gilmour painful blisters on her skin, mouth and esophagus. Courtesy of Charlotte Gilmour She said she has recovered but some symptoms ...

There is no standardized prediction system for Stevens-Johnson syndrome, which is rare. The model used included 216 ocular segment images from patients with chronic SJS and 50 from healthy patients.

Three years ago, in 2019, Cupay developed a rare skin disorder called Stevens-Johnson Syndrome which affects the skin and mucous membranes. Doctors say it could have killed her.

News Release 19-Feb-2025 Liver injury in immune Stevens-Johnson Syndrome and toxic epidermal necrolysis: Five new classification types Peer-Reviewed Publication Xia & He Publishing Inc. Introduction ...