Literature DB >> 18812929

Genetics of scoliosis.

Robert F Heary1, Karthik Madhavan.   

Abstract

Scoliosis is one of the oldest known deformities of humankind; however, the cause still remains ill defined. Although there is a lack of uniform agreement on the inclusion criteria for the definition of scoliosis, most investigators agree that a coronal curve must measure at least 10 degrees for the patient to be considered to have scoliosis. A broad range of articles were reviewed and the relevant publications that contributed information regarding the genetics of scoliosis were selected for inclusion in this report. Based on family pedigree and genetic studies, the proposed pattern of inheritance for markers of scoliosis are expected to be autosomal dominant, X-linked, multigene, or multifactorial. This is further complicated by locus heterogeneity, allele heterogeneity, and carrier states found in normal individuals. Although none of these modes of inheritance has been definitively proven, it appears that a multifactorial mode of inheritance with variable penetrance is the most likely method.

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Year:  2008        PMID: 18812929     DOI: 10.1227/01.NEU.0000320384.93384.28

Source DB:  PubMed          Journal:  Neurosurgery        ISSN: 0148-396X            Impact factor:   4.654


  5 in total

1.  Prospective evaluation of physical activity in patients with idiopathic scoliosis or kyphosis receiving brace treatment.

Authors:  Carsten Müller; Katharina Fuchs; Corinna Winter; Dieter Rosenbaum; Carolin Schmidt; Viola Bullmann; Tobias L Schulte
Journal:  Eur Spine J       Date:  2011-04-10       Impact factor: 3.134

2.  Severity of Idiopathic Scoliosis Is Associated with Differential Methylation: An Epigenome-Wide Association Study of Monozygotic Twins with Idiopathic Scoliosis.

Authors:  Patrick M Carry; Elizabeth A Terhune; George D Trahan; Lauren A Vanderlinden; Cambria I Wethey; Parvaneh Ebrahimi; Fiona McGuigan; Kristina Åkesson; Nancy Hadley-Miller
Journal:  Genes (Basel)       Date:  2021-07-30       Impact factor: 4.096

3.  Genetic markers for idiopathic scoliosis on chromosome 19p 13.3 among Saudi Arabian girls: A pilot study.

Authors:  Mir Sadat-Ali; Abdallah S Al-Omran; Abdallah A Al-Othman
Journal:  Indian J Hum Genet       Date:  2011-01

4.  ptk7 mutant zebrafish models of congenital and idiopathic scoliosis implicate dysregulated Wnt signalling in disease.

Authors:  Madeline Hayes; Xiaochong Gao; Lisa X Yu; Nandina Paria; R Mark Henkelman; Carol A Wise; Brian Ciruna
Journal:  Nat Commun       Date:  2014-09-03       Impact factor: 14.919

5.  Genetic Markers for Adolescent Idiopathic Scoliosis on Chromosome 19p13.3 among Saudi Arabian Girls.

Authors:  Abdallah Ahmad Al-Othman; Mir Sadat-Ali; Ahmed Sh Amer; Dakheel A Al-Dakheel
Journal:  Asian Spine J       Date:  2017-04-12
  5 in total

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