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Fraternal twins with job’s syndrome and immune complex nephritis
Job’s syndrome or autosomal dominant hyperimmunoglobulin E syndrome (Hyper-IgE) is a rare disorder that results from a STAT3 gene mutation, which results in the absence of T-helper 17 (Th17) cells and manifests as a severe immunodeficiency. Affected individuals suffer recurrent soft tissue and pulmo...
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| Publicado no: | CEN Case Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Japan
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5411662/ https://ncbi.nlm.nih.gov/pubmed/28509165 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-015-0191-0 |
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