Stevens-Johnson syndrome

Stevens-Johnson syndrome is a limited form of toxic epidermal necrolysis characterized by destruction and detachment of the skin epithelium and mucous membranes involving less than 10% of the body surface area.

Also known as: Dermatostomatitis, Stevens Johnson type, Stevens Johnson syndrome, Stevens-Johnson syndrome, susceptibility to, erythema multiforme major, hypersensitivity syndrome, carbamazepine-induced, susceptibility to, severe cutaneous adverse reaction, susceptibility to, toxic Epidermal necrolysis, susceptibility to

9 clinical trials for this condition and its sub-types, 9 tagged with Stevens-Johnson syndrome itself.