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Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series
BACKGROUND: Spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord is better known as herniated spinal cord. There are many arguments in favour of considering it a developmental defect. From this point of view, it is a type of neural tube disorder. Neural tube disorders can be c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132931/ https://www.ncbi.nlm.nih.gov/pubmed/32252670 http://dx.doi.org/10.1186/s12883-020-01710-7 |
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author | Bartels, Ronald H. M. A. Grotenhuis, J. Andre Stegmann, Alexander P. A. Brunner, Han |
author_facet | Bartels, Ronald H. M. A. Grotenhuis, J. Andre Stegmann, Alexander P. A. Brunner, Han |
author_sort | Bartels, Ronald H. M. A. |
collection | PubMed |
description | BACKGROUND: Spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord is better known as herniated spinal cord. There are many arguments in favour of considering it a developmental defect. From this point of view, it is a type of neural tube disorder. Neural tube disorders can be caused by multiple factors, including a genetic factor. A common genetic defect in patients with a spinal dysraphism with a hamartomatous growth of the spinal cord is sought for. CASE PRESENTATION: In two patients with a symptomatic lesion and referred to an academic hospital a genetic analysis was performed after informed consent. Whole-exome analysis was performed. : Whole-exome analysis did not result in identification of a clinically relevant genetic variant. CONCLUSIONS: This the first study to investigate the genetic contribution to spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord. We could not establish a genetic cause for this entity. This conclusion cannot be definitive due to the small sample size. However, the incidental occurrence, the lack of reports of inheritance of this disorder and the absence of contribution to syndromal disorders favours a defect of normal development of the spinal cord. |
format | Online Article Text |
id | pubmed-7132931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71329312020-04-11 Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series Bartels, Ronald H. M. A. Grotenhuis, J. Andre Stegmann, Alexander P. A. Brunner, Han BMC Neurol Case Report BACKGROUND: Spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord is better known as herniated spinal cord. There are many arguments in favour of considering it a developmental defect. From this point of view, it is a type of neural tube disorder. Neural tube disorders can be caused by multiple factors, including a genetic factor. A common genetic defect in patients with a spinal dysraphism with a hamartomatous growth of the spinal cord is sought for. CASE PRESENTATION: In two patients with a symptomatic lesion and referred to an academic hospital a genetic analysis was performed after informed consent. Whole-exome analysis was performed. : Whole-exome analysis did not result in identification of a clinically relevant genetic variant. CONCLUSIONS: This the first study to investigate the genetic contribution to spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord. We could not establish a genetic cause for this entity. This conclusion cannot be definitive due to the small sample size. However, the incidental occurrence, the lack of reports of inheritance of this disorder and the absence of contribution to syndromal disorders favours a defect of normal development of the spinal cord. BioMed Central 2020-04-06 /pmc/articles/PMC7132931/ /pubmed/32252670 http://dx.doi.org/10.1186/s12883-020-01710-7 Text en © The Author(s) 2020 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 | Case Report Bartels, Ronald H. M. A. Grotenhuis, J. Andre Stegmann, Alexander P. A. Brunner, Han Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series |
title | Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series |
title_full | Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series |
title_fullStr | Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series |
title_full_unstemmed | Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series |
title_short | Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series |
title_sort | genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132931/ https://www.ncbi.nlm.nih.gov/pubmed/32252670 http://dx.doi.org/10.1186/s12883-020-01710-7 |
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