Molecular diagnosis of vertebral segmentation disorders in humans

Philip F. Giampietro, Sally L. Dunwoodie, Kenro Kusumi, Olivier Pourquié, Olivier Tassy, Amaka C. Offiah, Alberto S. Cornier, Benjamin A. Alman, Robert D. Blank, Cathleen L. Raggio, Ingrid Glurich, Peter D. Turnpenny

Research output: Contribution to journalReview article

3 Scopus citations

Abstract

Background: Vertebral malformations contribute substantially to the pathophysiology of kyphosis and scoliosis, common health problems associated with back and neck pain, disability, cosmetic disfigurement and functional distress. Objective: To provide an overview of the current understanding of vertebral malformations, at both the clinical level and the molecular level, and factors that contribute to their occurrence. Methods: The literature related to the following was reviewed: recent advances in the understanding of the molecular embryology underlying vertebral development and relevance to elucidation of etiologies of several known human vertebral malformation syndromes; outcomes of molecular studies elucidating genetic contributions to congenital and sporadic vertebral malformations; and complex interrelationships between genetic and environmental factors that contribute to the pathogenesis of isolated syndromic and non-syndromic congenital vertebral malformations. Results/conclusion: Expert opinions extend to discussion of the importance of establishing improved classification systems for vertebral malformation, future directions in molecular and genetic research approaches to vertebral malformation and translational value of research efforts to clinical management and genetic counseling of affected individuals and their families.

Original languageEnglish (US)
Pages (from-to)1107-1121
Number of pages15
JournalExpert Opinion on Medical Diagnostics
Volume2
Issue number10
DOIs
StatePublished - Oct 1 2008

Keywords

  • Alagille syndrome
  • Array-based comparative genomic hybridization
  • CHARGE syndrome
  • CHD7
  • Congenital scoliosis
  • Congenital vertebral malformation
  • Dll3
  • ICVAS
  • JAG1
  • Jarcho Levin syndrome
  • Klippel-Feil syndrome
  • LFNG
  • MESP2
  • NOTCH2
  • PAX1
  • SLC35A3
  • Spondylothoracic dysostosis
  • T(Brachyury)
  • Tbx6
  • Teratogens
  • VACTERL
  • Wnt3A

ASJC Scopus subject areas

  • Biomedical Engineering
  • Molecular Medicine
  • Biochemistry, medical

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    Giampietro, P. F., Dunwoodie, S. L., Kusumi, K., Pourquié, O., Tassy, O., Offiah, A. C., Cornier, A. S., Alman, B. A., Blank, R. D., Raggio, C. L., Glurich, I., & Turnpenny, P. D. (2008). Molecular diagnosis of vertebral segmentation disorders in humans. Expert Opinion on Medical Diagnostics, 2(10), 1107-1121. https://doi.org/10.1517/17530059.2.10.1107