December 2015. Volume 11. Number 4

¿Es útil la prueba de ADN fetal libre de células para el diagnóstico de síndrome de Down?

 
 
 
 
 
 
 
 
 
 
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CA | Associated comment

Author: Santiago García FA1.
1Universidad Autónoma de Madrid . España.
Correspondence: Fe Amalia Santiago García. Email: feamalia.garcia@salud.madrid.org
Publication date: 23/09/2015

CA | Associated comment

Author: Santiago García FA1.
1Universidad Autónoma de Madrid . España.
Correspondence: Fe Amalia Santiago García. Email: feamalia.garcia@salud.madrid.org
Publication date: 23/09/2015

How to cite this article

García Santiago FA. ¿Es útil la prueba de ADN fetal libre de células para el diagnóstico de síndrome de Down? Evid Pediatr. 2015;11:66.

References

  1. Swanson A, Sehnert AJ, Bhatt S. Non-invasive prenatal testing: technologies, clinical assays and implementation strategies for women's healthcare practitioners. Curr Genet Med Rep. 2013;1:113-21.
  2. Lo YM, Corbetta N, Chamberlain PF, Rai V, Sargent IL, Redman CW, et al. Presence of fetal DNA in maternal plasma and serum. Lancet. 1997;350:485-7.
  3. Sparks AB, Wang ET, Struble CA, Barret W, Stokowski R, McBride C, et al. Selective analysis of cell-freeNA in maternal blood for evaluation of fetal trisomy. Prenat Diagn. 2012;32:3-9.
  4. Bianchi DW, Parker RL, Wentworth J,Madankumar R, Saffer C, Das AF, et al. DNA sequencing versus standard prenatal aneuploidy screening. N Engl J Med. 2014; 370: 799-808.
  5. Syngelaki A, Pergament E, Homfray T, Alokekar R, Nicolaides KH. Replacing the combined test by cell-free DNA testing in screening for trisomies 21, 18 and 13: impact on the diagnosis of other chromosomal abnormalities. Fetal Diagn Ther. 2014; 35:174-84.

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Aizpura Galdeano P, Orejón de Luna G. La prueba de ADN fetal libre de células, alternativa para el diagnóstico prenatal no invasivo del síndrome de Down. Evid Pediatr. 2015;11:57.
23/09/2015

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