Hemophilia A other diagnostic studies: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Hemophilia A}} | {{Hemophilia A}} | ||
{{CMG}} | {{CMG}}{{AE}}{{FNY}} {{VE}} | ||
==Overview== | ==Overview== | ||
[[Genetic testing]] appears to be a promising means of determining an individual's risk of attaining or passing on [[Hemophilia A|Hemophilia]] . | |||
==Other Diagnostic Studies== | ==Other Diagnostic Studies== | ||
Recently, | 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<ref name="pmid23932837">{{cite journal| author=Tsai MC, Cheng CN, Wang RJ, Chen KT, Kuo MC, Lin SJ| title=Cost-effectiveness analysis of carrier and prenatal genetic testing for X-linked hemophilia. | journal=J Formos Med Assoc | year= 2015 | volume= 114 | issue= 8 | pages= 722-8 | pmid=23932837 | doi=10.1016/j.jfma.2013.06.017 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23932837 }}</ref><ref name="pmid24762276">{{cite journal| author=de Brasi C, El-Maarri O, Perry DJ, Oldenburg J, Pezeshkpoor B, Goodeve A| title=Genetic testing in bleeding disorders. | journal=Haemophilia | year= 2014 | volume= 20 Suppl 4 | issue= | pages= 54-8 | pmid=24762276 | doi=10.1111/hae.12409 | pmc=4274362 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24762276 }}</ref>. | ||
==References== | ==References== | ||
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Latest revision as of 09:26, 29 January 2019
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Hemophilia A Microchapters |
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Treatment |
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Case Studies |
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Hemophilia A other diagnostic studies On the Web |
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American Roentgen Ray Society Images of Hemophilia A other diagnostic studies |
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Risk calculators and risk factors for Hemophilia A other diagnostic studies |
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.