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Genetic basis for iMCD-TAFRO
TAFRO syndrome, a clinical subtype of idiopathic multicentric Castleman disease (iMCD), consists of a constellation of symptoms/signs including thrombocytopenia, anasarca, fever, reticulin fibrosis/renal dysfunction, and organomegaly. The etiology of iMCD-TAFRO and the basis for cytokine hypersecret...
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| Publicado no: | Oncogene |
|---|---|
| Main Authors: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7148173/ https://ncbi.nlm.nih.gov/pubmed/32051554 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41388-020-1204-9 |
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