Etiology of Idiopathic Scoliosis: Current Trends in Research

Current population studies characterize idiopathic scoliosis as a single-gene disorder that follows the patterns of mendelian genetics, including variable penetrance and heterogeneity. The role of melatonin and calmodulin in the development of idiopathic scoliosis is likely secondary, with indirect...

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Published inJournal of bone and joint surgery. American volume Vol. 82; no. 8; p. 1157
Main Authors Lowe, Thomas G, Edgar, Michael, Margulies, Joseph Y, Miller, Nancy H, Raso, V James, Reinker, Kent A, Rivard, Charles-Hilaire
Format Journal Article
LanguageEnglish
Published Boston, MA Copyright by The Journal of Bone and Joint Surgery, Incorporated 01.08.2000
Journal of Bone and Joint Surgery Incorporated
Journal of Bone and Joint Surgery AMERICAN VOLUME
EditionAmerican volume
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Summary:Current population studies characterize idiopathic scoliosis as a single-gene disorder that follows the patterns of mendelian genetics, including variable penetrance and heterogeneity. The role of melatonin and calmodulin in the development of idiopathic scoliosis is likely secondary, with indirect effects on growth mechanisms. Reported abnormalities of connective tissue, skeletal muscle, platelets, the spinal column, and the rib cage are all thought to be secondary to the deformity itself. Although no consistent neurological abnormalities have been identified in patients with idiopathic scoliosis, it is possible that a defect in processing by the central nervous system affects the growing spine. The true etiology of idiopathic scoliosis remains unknown; however, it appears to be multifactorial.
Bibliography:ObjectType-Article-2
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ISSN:0021-9355
1535-1386
DOI:10.2106/00004623-200008000-00014