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Diagnostic workup of inherited platelet disorders
Blood Research ; : S11-S19, 2022.
Article en En | WPRIM | ID: wpr-925635
Biblioteca responsable: WPRO
ABSTRACT
Inherited platelet disorders (IPDs) can cause mucocutaneous bleeding due to impaired primary hemostatic function of platelets, thrombocytopenia, or both. Recent advances in molecular technology can help identify many genes related to platelet biology, control the overall steps of megakaryopoiesis, and cause IPD. In this article, currently available laboratory tools for diagnosing IPDs with the characteristic laboratory features of each IPD are reviewed, and a general diagnostic approach for the evaluation of IPD patients is presented.
Texto completo: 1 Base de datos: WPRIM Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Blood Research Año: 2022 Tipo del documento: Article
Texto completo: 1 Base de datos: WPRIM Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Blood Research Año: 2022 Tipo del documento: Article