Hemophilia A other diagnostic studies
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Fahd Yunus, M.D. [2] Vahid Eidkhani, M.D.
Overview
Genetic testing appears to be a promising means of determining an individual's risk of attaining or passing on Hemophilia .
Other Diagnostic Studies
Recently, genetic testing has been made available to determine an individual's risk of attaining or passing on Hemophilia. However this testing is still not standard of practice and is only available at limited centers[1][2].
References
- ↑ Tsai MC, Cheng CN, Wang RJ, Chen KT, Kuo MC, Lin SJ (2015). "Cost-effectiveness analysis of carrier and prenatal genetic testing for X-linked hemophilia". J Formos Med Assoc. 114 (8): 722–8. doi:10.1016/j.jfma.2013.06.017. PMID 23932837.
- ↑ de Brasi C, El-Maarri O, Perry DJ, Oldenburg J, Pezeshkpoor B, Goodeve A (2014). "Genetic testing in bleeding disorders". Haemophilia. 20 Suppl 4: 54–8. doi:10.1111/hae.12409. PMC 4274362. PMID 24762276.