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Dramatic Response of Familial Majeed Syndrome to Interleukin-1 Antagonist Therapy: Case report
Majeed syndrome (MS) is a rare, autosomal recessive, autoinflammatory disease characterized by recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and inflammatory dermatome. In this article, we report the cases of two siblings with MS. Genetic studies of both siblings were obta...
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| Publicat a: | Arch Rheumatol |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Turkish League Against Rheumatism
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6768791/ https://ncbi.nlm.nih.gov/pubmed/31598604 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5606/ArchRheumatol.2019.7267 |
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