Prenatal Diagnosis of Unbalanced Translocation t(5;11)(q21;q22) With a Jacobsen Syndrome Clinical Phenotype
This case report describes a fetus with a Jacobsen syndrome phenotype, caused by an unbalanced translocation t(5;11)(q21;q22) resulting from an inherited balanced translocation from one of the parents; it underscores the importance of undertaking prenatal diagnosis and genetic counseling in parents to help plan for future pregnancies.
Authors
- Shoko Miura
- Yuri Hasegawa (ORCID: https://orcid.org/0000-0002-9584-0023)
- Kiyonori Miura (ORCID: https://orcid.org/0000-0001-5396-8881)
- Yuriko Kitajima
- Koh Nagata
Institutions
- Nagasaki University (JP)
Publication Details
- Journal
- Clinical Case Reports
- Published
- 2025-08-01
- DOI
- https://doi.org/10.1002/ccr3.70772
- Primary Topic
- Genomic variations and chromosomal abnormalities
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Society for the Promotion of Science