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Publikováno v:
Diagnostics, Vol 14, Iss 10, p 1025 (2024)
TAFRO syndrome (TS) is a recently recognized and heterogenous systemic disease characterized by a confluence of symptoms: thrombocytopenia (T), anasarca (A), fever (F), reticulin myelofibrosis (R), and organomegaly (O). First described in Japan in 20
Externí odkaz:
https://doaj.org/article/2e5ad231a58342f58581286395fbe0d0