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A Case of Sporadic Blau Syndrome with an Uncommon Clinical Course
BACKGROUND: Sporadic Blau syndrome (SBS), a rare systemic inflammatory disease in children, is associated with NOD2 gene mutations. SBS is often misdiagnosed as juvenile idiopathic arthritis (JIA) because of their similar clinical manifestations. Herein, we present a case of SBS with an uncommon cli...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Hindawi
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332973/ https://www.ncbi.nlm.nih.gov/pubmed/30693132 http://dx.doi.org/10.1155/2018/6292308 |