Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16–18, 2017, Dallas, Texas. Issue 1 (21st November 2017)
- Record Type:
- Journal Article
- Title:
- Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16–18, 2017, Dallas, Texas. Issue 1 (21st November 2017)
- Main Title:
- Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16–18, 2017, Dallas, Texas
- Authors:
- Giampietro, Philip F.
Pourquie, Olivier
Raggio, Cathy
Ikegawa, Shiro
Turnpenny, Peter D.
Gray, Ryan
Dunwoodie, Sally L.
Gurnett, Christina A.
Alman, Benjamin
Cheung, Kenneth
Kusumi, Kenro
Hadley‐Miller, Nancy
Wise, Carol A. - Abstract:
- Abstract : Scoliosis represents the most common musculoskeletal disorder in children and affects approximately 3% of the world population. Scoliosis is separated into two major phenotypic classifications: congenital and idiopathic. Idiopathic scoliosis is defined as a curvature of the spine of 10° or greater visualized on plane radiograph and does not have associated vertebral malformations (VM). "Congenital" scoliosis (CS) due to malformations in vertebrae is frequently associated with other birth defects. Recently, significant advances have been made in understanding the genetic basis of both conditions. There is evidence that both conditions are etiologically related. A 2‐day conference entitled "Genomic Approaches to Understanding and Treating Scoliosis" was held at Scottish Rite Hospital for Children in Dallas, Texas, to synergize research in this field. This first combined, multidisciplinary conference featured international scoliosis researchers in basic and clinical sciences. A major outcome of the conference advancing scoliosis research was the proposal and subsequent vote in favor of merging the International Consortium for Vertebral Anomalies and Scoliosis (ICVAS) and International Consortium for Scoliosis Genetics (ICSG) into a single entity called International Consortium for Spinal Genetics, Development, and Disease (ICSGDD). The ICSGDD is proposed to meet annually as a forum to synergize multidisciplinary spine deformity research.
- Is Part Of:
- American journal of medical genetics. Volume 176:Issue 1(2018)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 176:Issue 1(2018)
- Issue Display:
- Volume 176, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 176
- Issue:
- 1
- Issue Sort Value:
- 2018-0176-0001-0000
- Page Start:
- 253
- Page End:
- 256
- Publication Date:
- 2017-11-21
- Subjects:
- congenital scoliosis -- GWAS -- idiopathic scoliosis -- natural history -- phenotypic classification -- spine deformity
Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.38550 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5637.xml