Cargando…
Failure of NIPT to detect constitutional chromoanasynthesis involving chromosome 21 in a case of fetal hydrops—A case report
We report a case of a de novo ring 21 complex chromosomal rearrangement in a fetus presenting with hydrops. Noninvasive prenatal testing (NIPT) failed to detect the imbalance. This case highlights the need to understand the various limitations and strengths of NIPT technology when counseling patient...
Autores principales: | Bone, Kathleen, MacPherson, Melissa Jean, Chernos, Judy, Lauzon, Julie |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878046/ https://www.ncbi.nlm.nih.gov/pubmed/31788271 http://dx.doi.org/10.1002/ccr3.2369 |
Ejemplares similares
-
Application value of NIPT for uncommon fetal chromosomal abnormalities
por: Yin, Lianli, et al.
Publicado: (2020) -
Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant
por: Sabatini, Peter J. B., et al.
Publicado: (2018) -
Multiple Chromoanasynthesis in a Rare Case of Sporadic Renal Leiomyosarcoma: A Case Report
por: Anoshkin, Kirill Igorevich, et al.
Publicado: (2020) -
Application of Microarray-Based Comparative Genomic Hybridization in Prenatal and Postnatal Settings: Three Case Reports
por: Liu, Jing, et al.
Publicado: (2011) -
The changing pattern of fetal hydrops.
por: Wilson, D. C., et al.
Publicado: (1990)