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.

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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

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article

Prenatal Diagnosis of Unbalanced Translocation t(5;11)(q21;q22) With a Jacobsen Syndrome Clinical Phenotype

Shoko Miura, Yuri Hasegawa, Kiyonori Miura, Yuriko Kitajima et al.
Clinical Case Reports
Genomic variations and chromosomal abnormalities
article

Prenatal Diagnosis of Unbalanced Translocation t(5;11)(q21;q22) With a Jacobsen Syndrome Clinical Phenotype

Shoko Miura, Yuri Hasegawa, Kiyonori Miura, Yuriko Kitajima, Koh Nagata
article en

Abstract

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.

Clinical Case ReportsVol. 13(8)
Nagasaki University (JP)
Japan Society for the Promotion of Science
Good health and well-being
Openalex Percentile: Top 77%
Genomic variations and chromosomal abnormalities
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