Hemophilia A overview

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Fahd Yunus, M.D. [2]

Overview

Hemophilia A is a blood clotting disorder caused by a mutation of the factor VIII gene, leading to a deficiency in Factor VIII. It is the most common hemophilia. Inheritance is X-linked recessive; hence, males are affected while females are carriers or very rarely display a mild phenotype. 1 in 5,000 males are affected.

Historical Perspective

Hemophilia is sometimes referred to as “The Royal Disease”, as it affected many members of the English, German, Russian and Spanish monarchies in the 19th and 20th centuries.

References

1. History of Bleeding Disorders | National Hemophilia Foundation. Available at . Accessed on July 30, 2016
2. How is Hemophilia Diagnosed? – NHLBI, NIH. Available at . Accessed on July 30, 2016
3. Severity of Hemophilia – World Federation of Hemophilia. Available at . Accessed on July 30,2016
4. Facts | Hemophilia | NCBDDD | CDC. Available at . Accessed on July 30,2016
5. Data & Statistics | Hemophilia | NCBDDD | CDC. Available at Accessed on July 30,2016
6. Handbook of Genetic Counseling/Hemophilia and Von Willebrand Disease – Wikibooks, open books for an open world. Available at Accessed on July 30,2016
7. Konkle BA, Josephson NC, Nakaya Fletcher S. Hemophilia A. 2000 Sep 21 [Updated 2014 Jun 5]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016. Available from:http://www-ncbi-nlm-nih-gov.laneproxy.stanford.edu/books/NBK1404/