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Stevens-Johnson syndrome

   Also found in: Medical, Encyclopedia, Wikipedia 0.01 sec.
Ste·vens-John·son syndrome  (stvnz-jnsn)
n.
A severe inflammatory eruption of the skin and mucous membranes, usually occurring in children and young adults following a respiratory infection or as an allergic reaction to drugs or other substances.

[After Albert Mason Stevens (1884-1945) and Frank Chambliss Johnson (1894-1934), American pediatricians.]


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Sharron "Kay" Thornton, from the southern US state of Mississippi, lost her sight in 2000 when she came down with a case of Stevens-Johnson syndrome, a rare disease that scarred her cornea, according to the University of Miami's Bascom Palmer Eye Institute.
Sharron "Kay" Thornton, from the southern US state of Mississippi, lost her sight in 2000 when she came down with a case of Stevens-Johnson syndrome, a rare disease that scarred her cornea, according to the University of Miami's Bascom Palmer Eye Institute.
The 14-year-old has Stevens-Johnson syndrome - a painful condition that covers the body in blisters and boils and can cause blindness, organ failure and, on rare occasions, death.
 
 
 
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