Immune Thrombocytopenic Purpura as a Hemorrhagic Versus Thrombotic Disease: An Updated Insight into Pathophysiological Mechanisms

Immune Thrombocytopenic Purpura as a Hemorrhagic Versus Thrombotic Disease: An Updated Insight into Pathophysiological Mechanisms

Immune thrombocytopenic purpura (ITP) is a blood disorder characterized by a low platelet count of (less than 100 × 10<sup>9</sup>/L). ITP is an organ-specific autoimmune disease in which the platelets and their precursors become targets of a dysfunctional immune system. This interaction...

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Bibliographic Details
Main Authors: Claudia Cristina Tărniceriu, Loredana Liliana Hurjui, Irina Daniela Florea, Ion Hurjui, Irina Gradinaru, Daniela Maria Tanase, Carmen Delianu, Anca Haisan, Ludmila Lozneanu
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Medicina
Subjects:
immune thrombocytopenic purpura (ITP)
thrombosis
hemorrhagic disease
regulatory cells
ITP treatment
Online Access:https://www.mdpi.com/1648-9144/58/2/211

Internet

https://www.mdpi.com/1648-9144/58/2/211

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