P538: Carrier risk assessment: Who gets it and where do they get it?
Abstract
Guidelines for carrier screening, particularly Tier 1 screening, have moved from racially and ethnicity specific approaches to uniform screening. Yet, disparities in access to parental heterozygote risk assessment are prevalent, and barriers to offering carrier screening remain unclear. The purpose of this study is to evaluate factors associated with completion of heterozygote risk assessment during pregnancy at a quaternary care referral center.
Fields of Study & Subjects
Prenatal Screening and Diagnostics
Metabolism and Genetic Disorders
Genomics and Rare Diseases
Publication details
- Journal / source
- Genetics in Medicine Open
- Volume
- 4
- Pages
- 104030–104030
- Publication date
- 1 January 2026
- Language
- EN