THROMBOCYTOPENIC PURPLE

dc.contributor.author	Umarkulov Muhtorali
dc.contributor.author	Xodjamberdiyev Akramjon
dc.contributor.author	Karimov Salohiddin
dc.date.accessioned	2025-12-31T15:35:51Z
dc.date.issued	2021-11-30
dc.description.abstract	Thrombocytopenic purpura (Werlhof's disease, benign thrombocytopenia) is a hematological pathology characterized by a quantitative deficiency of platelets in the blood, accompanied by a tendency to bleeding, the development of hemorrhagic syndrome. With thrombocytopenic purpura, the level of platelets in the peripheral blood drops significantly below the physiological level - 150x109 / l with a normal or slightly increased number of megakaryocytes in the bone marrow. In terms of the frequency of occurrence, thrombocytopenic purpura ranks first among another hemorrhagic diathesis
dc.format	application/pdf
dc.identifier.uri	https://scholarexpress.net/index.php/wbph/article/view/329
dc.identifier.uri	https://asianeducationindex.com/handle/123456789/48786
dc.language.iso	eng
dc.publisher	Scholar Express Journals
dc.relation	https://scholarexpress.net/index.php/wbph/article/view/329/325
dc.rights	https://creativecommons.org/licenses/by-nc-nd/4.0
dc.source	World Bulletin of Public Health; Vol. 4 (2021): WBPH; 125-127
dc.source	2749-3644
dc.subject	thrombocytopenias
dc.subject	Isoimmune
dc.subject	Transimmune
dc.subject	angiotrophic
dc.title	THROMBOCYTOPENIC PURPLE
dc.type	info:eu-repo/semantics/article
dc.type	info:eu-repo/semantics/publishedVersion
dc.type	Peer-reviewed Article

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