Literature DB >> 27645814

Cell-Free Fetal DNA Testing for Prenatal Diagnosis.

S Drury1, M Hill1, L S Chitty2.   

Abstract

Prenatal diagnosis and screening have undergone rapid development in recent years, with advances in molecular technology driving the change. Noninvasive prenatal testing (NIPT) for Down syndrome as a highly sensitive screening test is now available worldwide through the commercial sector with many countries moving toward implementation into their publically funded maternity systems. Noninvasive prenatal diagnosis (NIPD) can now be performed for definitive diagnosis of some recessive and X-linked conditions, rather than just paternally inherited dominant and de novo conditions. NIPD/T offers pregnant couples greater choice during their pregnancy as these safer methods avoid the risk of miscarriage associated with invasive testing. As the cost of sequencing falls and technology develops further, there may well be potential for whole exome and whole genome sequencing of the unborn fetus using cell-free DNA in the maternal plasma. How such assays can or should be implemented into the clinical setting remain an area of significant debate, but it is clear that the progress made to date for safer prenatal testing has been welcomed by expectant couples and their healthcare professionals.
© 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Aneuploidy; Cell-free DNA; NIPD; NIPT; Noninvasive prenatal diagnosis; Noninvasive prenatal testing; Single gene disorders; cffDNA

Mesh:

Substances:

Year:  2016        PMID: 27645814     DOI: 10.1016/bs.acc.2016.05.004

Source DB:  PubMed          Journal:  Adv Clin Chem        ISSN: 0065-2423            Impact factor:   5.394


  19 in total

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