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Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities
Background: Musculocontractural Ehlers–Danlos syndrome (mcEDS) is a rare heritable connective tissue disease with various symptoms. The diagnosis of mcEDS is difficult because of the large overlap of clinical symptoms between different EDS subtypes. Methods: We performed karyotype analysis, gene cop...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024400/ https://www.ncbi.nlm.nih.gov/pubmed/35464846 http://dx.doi.org/10.3389/fgene.2022.853907 |
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author | Zhou, Yuan-Yuan Du, Yu-Fang Lu, Qing Zhai, Xiu-Zhang Shi, Ming-Fang Chen, Dan-Yun Liu, Sun-Rong Zhong, Ying |
author_facet | Zhou, Yuan-Yuan Du, Yu-Fang Lu, Qing Zhai, Xiu-Zhang Shi, Ming-Fang Chen, Dan-Yun Liu, Sun-Rong Zhong, Ying |
author_sort | Zhou, Yuan-Yuan |
collection | PubMed |
description | Background: Musculocontractural Ehlers–Danlos syndrome (mcEDS) is a rare heritable connective tissue disease with various symptoms. The diagnosis of mcEDS is difficult because of the large overlap of clinical symptoms between different EDS subtypes. Methods: We performed karyotype analysis, gene copy number variation detection, whole-exome sequencing, and Sanger sequencing to reveal the underlying genetic etiology of a fetus with structural abnormalities in feet and kidneys. Results: A likely pathogenic mutation [NM_130468.3 c.958C>T (p.Arg320*)] and an uncertain significance mutation [NM_130468.3 c.896A>G (p.Tyr299Cys)] were identified in the carbohydrate sulfotransferase 14 (CHST14) gene by whole-exome sequencing and validated by Sanger sequencing. Conclusion: The two identified mutations appear highly likely to be the genetic causes of the fetal structural abnormalities. |
format | Online Article Text |
id | pubmed-9024400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90244002022-04-23 Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities Zhou, Yuan-Yuan Du, Yu-Fang Lu, Qing Zhai, Xiu-Zhang Shi, Ming-Fang Chen, Dan-Yun Liu, Sun-Rong Zhong, Ying Front Genet Genetics Background: Musculocontractural Ehlers–Danlos syndrome (mcEDS) is a rare heritable connective tissue disease with various symptoms. The diagnosis of mcEDS is difficult because of the large overlap of clinical symptoms between different EDS subtypes. Methods: We performed karyotype analysis, gene copy number variation detection, whole-exome sequencing, and Sanger sequencing to reveal the underlying genetic etiology of a fetus with structural abnormalities in feet and kidneys. Results: A likely pathogenic mutation [NM_130468.3 c.958C>T (p.Arg320*)] and an uncertain significance mutation [NM_130468.3 c.896A>G (p.Tyr299Cys)] were identified in the carbohydrate sulfotransferase 14 (CHST14) gene by whole-exome sequencing and validated by Sanger sequencing. Conclusion: The two identified mutations appear highly likely to be the genetic causes of the fetal structural abnormalities. Frontiers Media S.A. 2022-04-08 /pmc/articles/PMC9024400/ /pubmed/35464846 http://dx.doi.org/10.3389/fgene.2022.853907 Text en Copyright © 2022 Zhou, Du, Lu, Zhai, Shi, Chen, Liu and Zhong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Zhou, Yuan-Yuan Du, Yu-Fang Lu, Qing Zhai, Xiu-Zhang Shi, Ming-Fang Chen, Dan-Yun Liu, Sun-Rong Zhong, Ying Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities |
title | Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities |
title_full | Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities |
title_fullStr | Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities |
title_full_unstemmed | Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities |
title_short | Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities |
title_sort | case report: a novel mutation identified in chst14 gene in a fetus with structural abnormalities |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024400/ https://www.ncbi.nlm.nih.gov/pubmed/35464846 http://dx.doi.org/10.3389/fgene.2022.853907 |
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