Coagulation and bleeding disorders

No Thumbnail Available
File version
Author(s)
Singh, I
Singh, RI
Griffith University Author(s)
Primary Supervisor
Other Supervisors
Editor(s)
Date
2019
Size
File type(s)
Location
License
Abstract

Thrombosis is a complex disorder involving interaction between many different types of genes with environment factors. Modification in genes coding for coagulation and regulatory proteins of hemostasis are important risk factors for thrombosis. Historically, the measurement of a clot endpoint has been the basis of coagulation testing mainly focused on bleeding disorders. Thrombosis diagnosis has slowly increased with most modern automated coagulation instruments utilizing optic, immunologic, and chromogenic methods. However, molecular diagnostics has added another dimension for the evaluation of clotting and bleeding disorders. DNA-based tests are commonly available for the detection of the factor V Leiden mutation, the prothrombin 20120A mutation, and the methyltetrahydrofolate reductase mutation.

Journal Title
Conference Title
Book Title

Clinical Molecular Medicine: Principles and Practice

Edition
Volume
Issue
Thesis Type
Degree Program
School
Publisher link
Patent number
Funder(s)
Grant identifier(s)
Rights Statement
Rights Statement

Self-archiving is not yet supported by this publisher. Please refer to the publisher's website or contact the author(s) for more information.

Item Access Status
Note
Access the data
Related item(s)
Subject

Biomedical and clinical sciences

Persistent link to this record
Citation

Singh, I; Singh, RI, Coagulation and bleeding disorders, Clinical Molecular Medicine: Principles and Practice, 2019, pp. 341-352

Collections