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Nature 428, 486 (1 April 2004) | doi:10.1038/428486a
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Medical genetics: A marker for Stevens–Johnson syndrome
Wen-Hung Chung1, Shuen-Iu Hung3, Hong-Shang Hong1, Mo-Song Hsih2, Li-Cheng Yang1, Hsin-Chun Ho1, Jer-Yuarn Wu3,4 & Yuan-Tsong Chen3,5
Abstract
Stevens–Johnson syndrome and the related disease toxic epidermal necrolysis are life-threatening reactions of the skin to particular types of medication1, 2, 3. Here we show that there is a strong association in Han Chinese between a genetic marker, the human leukocyte antigen HLA–B*1502, and Stevens–Johnson syndrome induced by carbamazepine, a drug commonly prescribed for the treatment of seizures. It should be possible to exploit this association in a highly reliable test to predict severe adverse reaction, as well as for investigation of the pathogenesis of Stevens–Johnson syndrome.
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RESEARCH
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Granulysin is a key mediator for disseminated keratinocyte death in Stevens-Johnson syndrome and toxic epidermal necrolysisNature Medicine Letter (01 Dec 2008)
Stevens?Johnson Syndrome and Toxic Epidermal Necrolysis: Assessment of Medication Risks with Emphasis on Recently Marketed Drugs. The EuroSCAR-StudyJournal of Investigative Dermatology Original Article
Nitric Oxide Synthase in Toxic Epidermal Necrolysis and Stevens?Johnson SyndromeJournal of Investigative Dermatology Commentary
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