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Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family
BACKGROUND: Distal 8p duplication is rare but clinically significant. Duplication syndrome results in variable phenotypes, such as developmental delay, intellectual disability, and malformation of the heart. We aimed to provide a better understanding of the phenotypes by studying duplication and its...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988938/ https://www.ncbi.nlm.nih.gov/pubmed/33757501 http://dx.doi.org/10.1186/s12920-021-00940-z |
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author | Shi, Panlai Wang, Conghui Zheng, Yuting Kong, Xiangdong |
author_facet | Shi, Panlai Wang, Conghui Zheng, Yuting Kong, Xiangdong |
author_sort | Shi, Panlai |
collection | PubMed |
description | BACKGROUND: Distal 8p duplication is rare but clinically significant. Duplication syndrome results in variable phenotypes, such as developmental delay, intellectual disability, and malformation of the heart. We aimed to provide a better understanding of the phenotypes by studying duplication and its effects in a single family. METHODS: In a family with a previously induced labor (second fetus) at 12 weeks gestation due to increased nuchal translucency (3.5 mm), copy number variation sequencing (CNV-seq) revealed a 16.22 Mb deletion of 8p23.3p22. For their subsequent pregnancy, the family requested a prenatal diagnosis as well as CNV-seq, karyotyping and FISH testing of all family members. RESULTS: The first and third children were found to have a 16.22 Mb duplication of 8p23.3p22, containing the 8p23.1 duplication syndrome region. The duplication was inherited from their father, a carrier with a translocation of 8p22 and 22q13. We confirmed that the duplication site was located on chromosome 22q13 by combining the results of CNV-seq, karyotype and FISH. The first child is a 7.5-year-old boy. At one month old, he was diagnosed with a ventricular septal defect and treated surgically at age four. His growth and intelligence developed well, and he performed well in school. His primary issue is an inability to distinguish between the blade alveolars and retroflexes in speech. The third fetus had a normal ultrasound index from beginning until birth. The family elected to continue the pregnancy, and the baby was born healthy, providing us the opportunity to evaluate the effects of 8p23.3p22 duplication by comparison with the brother. CONCLUSION: Our study makes a significant contribution to the literature because this relatively rare condition can have significant phenotypical consequences, and an understanding of the inheritance and variability of phenotypes caused by this mutation is essential to an increased understanding of the condition. |
format | Online Article Text |
id | pubmed-7988938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79889382021-03-25 Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family Shi, Panlai Wang, Conghui Zheng, Yuting Kong, Xiangdong BMC Med Genomics Research Article BACKGROUND: Distal 8p duplication is rare but clinically significant. Duplication syndrome results in variable phenotypes, such as developmental delay, intellectual disability, and malformation of the heart. We aimed to provide a better understanding of the phenotypes by studying duplication and its effects in a single family. METHODS: In a family with a previously induced labor (second fetus) at 12 weeks gestation due to increased nuchal translucency (3.5 mm), copy number variation sequencing (CNV-seq) revealed a 16.22 Mb deletion of 8p23.3p22. For their subsequent pregnancy, the family requested a prenatal diagnosis as well as CNV-seq, karyotyping and FISH testing of all family members. RESULTS: The first and third children were found to have a 16.22 Mb duplication of 8p23.3p22, containing the 8p23.1 duplication syndrome region. The duplication was inherited from their father, a carrier with a translocation of 8p22 and 22q13. We confirmed that the duplication site was located on chromosome 22q13 by combining the results of CNV-seq, karyotype and FISH. The first child is a 7.5-year-old boy. At one month old, he was diagnosed with a ventricular septal defect and treated surgically at age four. His growth and intelligence developed well, and he performed well in school. His primary issue is an inability to distinguish between the blade alveolars and retroflexes in speech. The third fetus had a normal ultrasound index from beginning until birth. The family elected to continue the pregnancy, and the baby was born healthy, providing us the opportunity to evaluate the effects of 8p23.3p22 duplication by comparison with the brother. CONCLUSION: Our study makes a significant contribution to the literature because this relatively rare condition can have significant phenotypical consequences, and an understanding of the inheritance and variability of phenotypes caused by this mutation is essential to an increased understanding of the condition. BioMed Central 2021-03-23 /pmc/articles/PMC7988938/ /pubmed/33757501 http://dx.doi.org/10.1186/s12920-021-00940-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Shi, Panlai Wang, Conghui Zheng, Yuting Kong, Xiangdong Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family |
title | Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family |
title_full | Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family |
title_fullStr | Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family |
title_full_unstemmed | Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family |
title_short | Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family |
title_sort | prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988938/ https://www.ncbi.nlm.nih.gov/pubmed/33757501 http://dx.doi.org/10.1186/s12920-021-00940-z |
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