Omenn's syndrome


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O·menn's syndrome

(ō′mĕnz′)
n.
A rapidly fatal familial immunodeficiency disease characterized by widespread reddening of the skin, diarrhea, repeated infections, enlargement of the liver and spleen, and leukocytosis.
The American Heritage® Medical Dictionary Copyright © 2007, 2004 by Houghton Mifflin Company. Published by Houghton Mifflin Company. All rights reserved.
References in periodicals archive ?
Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).