Factor X Deficiency

Factor X Deficiency

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Factor X Deficiency

Deborah Brown, MD* and Peter A. Kouides, MD

*Correspondence: deborah.brown@uth.tmc.edu

Manuscript modified from original article published in Haemophilia 2008 (Brown DL, Kouides PA. Diagnosis and treatment of inherited factor X deficiency. Haemophilia. 2008; 14, 1176–1182.)

Disease Overview
Pattern of Inheritance
Clinical Presentation
Differential Diagnosis
Laboratory Evaluation
Medications/Treatment
Research
Resources
References

Acknowledgment

The Rare Coagulation Disorders Resource Room, an extension of the RBDD Registry (http://eu.rbdd.org/), was developed in collaboration with the Indiana Hemophilia & Thrombosis Center (www.ihtc.org).

The Resource Room serves as a platform to promote international collaboration to increase knowledge of these very rare disorders and to improve the care of affected individuals. The international RBDD mission, under the leadership of Dr. Peyvandi, will continue to be expanded over time.

The Resource Room thanks all contributing authors of the website articles that have made this valuable information available to the global community of both individuals affected with rare coagulation disorders and their health care providers.

A collaboration of RBDD and IHTC

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