Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series

R.H.M.A. Bartels*, J.A. Grotenhuis, A.P.A. Stegmann, H. Brunner

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

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.
Original languageEnglish
Article number121
Number of pages4
JournalBMC Neurology
Volume20
Issue number1
DOIs
Publication statusPublished - 6 Apr 2020

Keywords

  • abnormal development
  • case series
  • genetic analysis
  • herniation
  • specification
  • spinal cord
  • Spinal cord
  • Abnormal development
  • Genetic analysis
  • HERNIATION
  • Case series
  • SPECIFICATION

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