Mean platelet volume for distinguishing between inherited thrombocytopenias and immune thrombocytopenia - response to Beyan

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Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study

The most frequent forms of inherited thrombocytopenia (IT) are characterized by platelet size abnormalities and it has been suggested that this parameter is useful for their differentiation from immune thrombocytopenia (ITP). Recently, a monocentric study identified cut-off values for mean platelet volume (MPV) and mean platelet diameter (MPD) with good diagnostic accuracy in this respect. To v...

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Mean Platelet Volume (MPV) in Thrombocytopenia

Background: The platelet volume parameters have been widely available as part of full blood count profile on automated haematology analyzers. However, the mean platelet volume (MPV) and other platelet indices are used less often and are poorly understood. Platelet volume data is generated at no extra cost as part of full blood count profile. Low platelet counts can have myriad cause which can b...

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Inherited thrombocytopenias.

Bleeding syndromes that arise through an inherited defect of platelet production constitute a heterogeneous group of rare platelet disorders of growing importance. Some, including the Bernard-Soulier syndrome (BSS) and Wiskott-Aldrich syndrome (WAS), associate a low circulating platelet count with a deficiency in a known functional protein (Table 1). In others, platelet dysfunction has not been...

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Inherited thrombocytopenias.

Secondary causes of thrombocytopenia as immunologic thrombopenia purpura, or ITP, are far more common than inherited causes, which even as a group, are rare. Nevertheless, diagnosis is important and progress made in uncovering the molecular basis of these disorders has contributed greatly to our knowledge of these diseases. Inherited thrombocytopenias are a heterogeneous group of disorders. Dif...

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ژورنال

عنوان ژورنال: British Journal of Haematology

سال: 2013

ISSN: 0007-1048

DOI: 10.1111/bjh.12504