Severe combined immunodeficiency with hypereosinophilia (Q56061): Difference between revisions
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Síndrome de Omenn (OS) é uma condição inflamatória caracterizada por eritrodermia, descamação, alopécia, diarreia crônica, falha no crescimento, linfadenopatia e hepatoesplenomegalia, associados à imunodeficiência combinada grave (IDCG). | |||
| description / en | description / en | ||
Omenn syndrome (OS) is an inflammatory condition characterised by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; ). | |||
Revision as of 03:44, 14 August 2026
Omenn syndrome (OS) is an inflammatory condition characterised by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; ).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1770823271 |
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| English | Severe combined immunodeficiency with hypereosinophilia |
Omenn syndrome (OS) is an inflammatory condition characterised by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; ). |
