» Articles » PMID: 12151883

Genetics of Familial Idiopathic Scoliosis

Overview
Publisher Wolters Kluwer
Specialty Orthopedics
Date 2002 Aug 2
PMID 12151883
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

The etiology of familial idiopathic scoliosis is unknown. The role of genetic factors in the development of this disorder has been well documented; however, reports of the specific mode of genetic inheritance are inconclusive. These facts, combined with the phenotypic variability of this disorder suggest that the genetic expression of idiopathic scoliosis may be dependent on multiple factors and genetic interactions. Strategies to resolve the complex nature of this condition include genome-wide scanning of an extended family or, alternatively, a well-characterized population of families affected with idiopathic scoliosis.

Citing Articles

A Genetic Variant in GPR126 Causing a Decreased Inclusion of Exon 6 Is Associated with Cartilage Development in Adolescent Idiopathic Scoliosis Population.

Xu E, Shao W, Jiang H, Lin T, Gao R, Zhou X Biomed Res Int. 2019; 2019:4678969.

PMID: 30886859 PMC: 6388357. DOI: 10.1155/2019/4678969.


Association between polymorphisms in vitamin D receptor gene and adolescent idiopathic scoliosis: a meta-analysis.

Dai J, Lv Z, Huang J, Cheng P, Fang H, Chen A Eur Spine J. 2018; 27(9):2175-2183.

PMID: 29728923 DOI: 10.1007/s00586-018-5614-0.


Lack of association between AKAP2 and the susceptibility of adolescent idiopathic scoliosis in the Chinese population.

Xu L, Xia C, Zhu W, Feng Z, Qin X, Sun W BMC Musculoskelet Disord. 2017; 18(1):368.

PMID: 28838314 PMC: 5571670. DOI: 10.1186/s12891-017-1731-x.


Selective estrogen receptor modulation prevents scoliotic curve progression: radiologic and histomorphometric study on a bipedal C57Bl6 mice model.

Demirkiran G, Dede O, Yalcin N, Akel I, Marcucio R, Acaroglu E Eur Spine J. 2013; 23(2):455-62.

PMID: 24136418 PMC: 3906449. DOI: 10.1007/s00586-013-3072-2.


Familial or Sporadic Idiopathic Scoliosis - classification based on artificial neural network and GAPDH and ACTB transcription profile.

Waller T, Nowak R, Tkacz M, Zapart D, Mazurek U Biomed Eng Online. 2013; 12:1.

PMID: 23289769 PMC: 3599878. DOI: 10.1186/1475-925X-12-1.