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dc.contributor.author Dudnyk, V. M. en
dc.contributor.author Furman, V. G. en
dc.contributor.author Kutsak, O. V. en
dc.contributor.author Izyumets, O. I. en
dc.date.accessioned 2022-05-17T07:43:32Z
dc.date.available 2022-05-17T07:43:32Z
dc.date.issued 2022
dc.identifier.citation Heritable amegacariocytic thrombocytopenia: description of aclinical case / V. M. Dudnyk, V. G. Furman, O. V. Kutsak, O. I. Izyumets // Вісник Вінницького національного медичного університету. - 2022. - Т. 26, № 1. – C. 27-30. en
dc.identifier.uri https://dspace.vnmu.edu.ua/123456789/5644
dc.description.abstract Features of the clinical course and differential diagnosis of hereditary thrombocytopenia, characterized by the development of pancytopenia in childhood, are described. It was found that the main manifestation of this pathology is hemorrhagic syndrome, accompanied by the presence of polymorphic, polychrome, asymmetric hemorrhagic rashes, frequent bleeding from the mucous membranes. The Mpl gene (1p34) was sequestered to confirm the diagnosis and establish the genomic mutation. Complex diagnosis of this disease requires a comprehensive and interdisciplinary approach involving a coordinated team of hematologists, geneticists, immunologists, neurosurgeons and ophthalmologists. en
dc.language.iso en en
dc.subject children en
dc.subject thrombocytopenia en
dc.subject hemorrhagic syndrome en
dc.subject gen Mpl (1p34) en
dc.title Heritable amegacariocytic thrombocytopenia: description of aclinical case en
dc.type Article en


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