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A new case of 17p13.3p13.1 microduplication resulted from unbalanced translocation: clinical and molecular cytogenetic characterization

Title: A new case of 17p13.3p13.1 microduplication resulted from unbalanced translocation: clinical and molecular cytogenetic characterization
Authors: Zhanna G. Markova; Marina E. Minzhenkova; Lyudmila A. Bessonova; Nadezda V. Shilova
Source: Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-10 (2021)
Publisher Information: BMC
Publication Year: 2021
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: 17p13.3p13.1 microduplication; Chromosomal microarray analysis; FISH; Genetics; QH426-470
Description: Copy number gain 17 p13.3p13.1 was detected by chromosomal microarray (CMA) in a girl with developmental/speech delay and facial dysmorphism. FISH studies made it possible to establish that the identified genomic imbalance is the unbalanced t(9;17) translocation of maternal origin. Clinical features of the patient are also discussed. The advisability of using the combination of CMA and FISH analysis is shown. Copy number gains detected by clinical CMA should be confirmed using FISH analysis in order to determine the physical location of the duplicated segment. Parental follow-up studies is an important step to determine the origin of genomic imbalance. This approach not only allows a most comprehensive characterization of an identified chromosomal/genomic imbalance but also provision of an adequate medical and genetic counseling for a family taking into account a balanced chromosomal rearrangement.
Document Type: article in journal/newspaper
Language: English
Relation: https://doi.org/10.1186/s13039-021-00562-1; https://doaj.org/toc/1755-8166; https://doaj.org/article/b20dabdd1d7e4dcda985e42f0302774e
DOI: 10.1186/s13039-021-00562-1
Availability: https://doi.org/10.1186/s13039-021-00562-1; https://doaj.org/article/b20dabdd1d7e4dcda985e42f0302774e
Accession Number: edsbas.29C39F0A
Database: BASE