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Atypical Omenn Syndrome due to Adenosine Deaminase Deficiency
We present here a novel case of an atypical Omenn syndrome (OS) phenotype due to mutations in the ADA gene encoding adenosine deaminase. This case is noteworthy for a significant increase in circulating CD56(bright)CD16- cytokine-producing NK cells after treatment with steroids for skin rash.
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| Publicado no: | Case Reports Immunol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4412092/ https://ncbi.nlm.nih.gov/pubmed/25954555 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/919241 |
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