Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance. Issue 1 (6th October 2022)
- Record Type:
- Journal Article
- Title:
- Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance. Issue 1 (6th October 2022)
- Main Title:
- Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance
- Authors:
- Howell, Susan
Davis, Shanlee M.
Thompson, Talia
Brown, Mariah
Tanda, Tanea
Kowal, Karen
Alston, Amanda
Ross, Judith
Tartaglia, Nicole R. - Abstract:
- Abstract: Sex chromosome aneuploidies (SCAs), including 47, XXY, 47, XXX, 47, XYY, and supernumerary variants, occur collectively in approximately one of 500 live births. Clinical phenotypes are highly variable resulting in previous ascertainment rates estimated to be only 10%–25% during a lifetime. Historically, prenatal SCA diagnoses were incidental findings, accounting for ≤10% of cases, with the majority of diagnoses occurring postnatally during evaluations for neurodevelopmental, medical, or infertility concerns. The initiation of noninvasive prenatal screening (NIPS) in 2012 and adoption into standardized obstetric care provides a unique opportunity to significantly increase prenatal ascertainment of SCAs. However, the impact NIPS has had on ascertainment of SCAs is understudied, particularly for those who may defer diagnostic testing until after birth. This study evaluates the timing of diagnostic testing following positive NIPS in 152 infants with SCAs and potential factors influencing this decision. Eighty‐seven (57%) elected to defer diagnostic testing after a positive NIPS until birth, and 8% (7/87) of those confirmed after birth were found to have discordant results on postnatal diagnostic testing, most of which would have influenced genetic counseling.
- Is Part Of:
- Journal of genetic counseling. Volume 32:Issue 1(2023)
- Journal:
- Journal of genetic counseling
- Issue:
- Volume 32:Issue 1(2023)
- Issue Display:
- Volume 32, Issue 1 (2023)
- Year:
- 2023
- Volume:
- 32
- Issue:
- 1
- Issue Sort Value:
- 2023-0032-0001-0000
- Page Start:
- 250
- Page End:
- 259
- Publication Date:
- 2022-10-06
- Subjects:
- decision‐making -- genetic counseling -- genetic testing -- noninvasive prenatal screening -- prenatal diagnosis -- sex chromosome aneuploidy
Genetic counseling -- Periodicals
616.042 - Journal URLs:
- https://onlinelibrary.wiley.com/journal/15733599 ↗
http://www.springer.com/gb/ ↗ - DOI:
- 10.1002/jgc4.1639 ↗
- Languages:
- English
- ISSNs:
- 1059-7700
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4989.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25761.xml