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A Case of Omenn Syndrome in a Patient Treated for Chronic Diarrhea and Severe Exfoliative Erythrodermia

Yum MS, Lee SY, Kim HB, Yoo HW, Ghim T, Hong SJ

  • KMID: 2314377
  • Pediatr Allergy Respir Dis.
  • 2005 Jun;15(2):174-179.
Omenn syndrome (OS) is a peculiar, autosomal recessive severe combined immunodeficiency (SCID) associated with early-onset, generalized, exudative erythrodermia, lymphadenopathy, hepatosplenomegaly, hypereosinophilia, elevated serum IgE, and normal to highly activated, yet...
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