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Advance in the diagnosis and treatment of hereditary thrombotic thrombocytopenic purpura / 中华医学遗传学杂志
Article in Zh | WPRIM | ID: wpr-928438
Responsible library: WPRO
ABSTRACT
Congenital thrombotic thrombocytopenic purpura, also known as Upshaw-Schulman syndrome, is a rare autosomal recessive genetic disorder. The main pathogenesis is homozygous or compound heterozygous variants of von Willebrand factor lyase (ADAMTS13) gene mapped to chromosome 9q34, which may result in severe lack of ADAMTS13 which cleaves von Willebrand factor (vWF) multimers in the plasma and increase the risk of microvascular thrombosis, leading to various complications. The advance of research on the pathogenesis of cTTP, recombinant human ADAMTS13 and gene therapy have made breakthroughs which may lead to cure of cTTP. This article has provided a review for the latest progress made in the diagnosis and treatment of cTTP.
Subject(s)
Full text: 1 Index: WPRIM Main subject: Purpura, Thrombotic Thrombocytopenic / Von Willebrand Factor / ADAM Proteins / ADAMTS13 Protein / Homozygote Type of study: Diagnostic_studies Limits: Humans Language: Zh Journal: Chinese Journal of Medical Genetics Year: 2022 Type: Article
Full text: 1 Index: WPRIM Main subject: Purpura, Thrombotic Thrombocytopenic / Von Willebrand Factor / ADAM Proteins / ADAMTS13 Protein / Homozygote Type of study: Diagnostic_studies Limits: Humans Language: Zh Journal: Chinese Journal of Medical Genetics Year: 2022 Type: Article