Medical Findings in Infants Prenatally Identified With Sex Chromosome Trisomy in Year 1 of Life
Results inform care as pediatricians and families can be reassured that a prenatal diagnosis of SCT is not associated with complex medical or physical abnormalities within the first year of life, but proactive monitoring for select at-risk conditions is warranted.
Authors
- Shanlee Davis (ORCID: https://orcid.org/0000-0002-0304-9550)
- Samantha Bothwell (ORCID: https://orcid.org/0000-0002-1616-8137)
- Karen Kowal
- Susan Howell (ORCID: https://orcid.org/0000-0001-7115-2165)
- Chijioke Ikomi (ORCID: https://orcid.org/0000-0002-0630-2355)
- Agnethe Berglund (ORCID: https://orcid.org/0000-0001-9185-1342)
- Judith L. Ross (ORCID: https://orcid.org/0000-0002-8613-2498)
- Kayla Nocon (ORCID: https://orcid.org/0009-0007-4974-9089)
- Andrew Keene (ORCID: https://orcid.org/0009-0008-7317-3064)
- Nicole Tartaglia
- Victoria Reynolds
Institutions
- Alfred I. duPont Hospital for Children (US)
- Community Health Systems - Dupont Hospital (US)
- Aarhus University Hospital (DK)
- Children's Hospital Colorado (US)
- Nemours Children's Health System (US)
- University of Colorado Denver (US)
Publication Details
- Journal
- PEDIATRICS
- Published
- 2025-09-26
- DOI
- https://doi.org/10.1542/peds.2024-068133
- Primary Topic
- Prenatal Screening and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 0.00