Omenn syndrom
Engelsk navn: Omenn syndrome
Engelske synonym: Combined immunodeficiency with hypereosinophilia
Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; see this term).
Informasjon
Senter for sjeldne diagnoser ved OUS har kunnskap om diagnosen.
ORPHA: 39041
Klassifiseringsnivå: DisorderICD-10: D81.8