Congenital Kyphosis And Kyphoscoliosis: The Natural History And Results After Surgery

Congenital kyphosis and kyphoscoliosis are due to vertebral anomalies that are present at birth. These vertebral anomalies cause a deformity of the spine in the sagittal plane. If allowed to progress, this deformity can produce neural dysfunction due to bowstringing of the cord over the apex of t...

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Main Author: Singh, Harwant
Format: Thesis
Language:English
English
Published: 2000
Online Access:http://psasir.upm.edu.my/id/eprint/11267/1/FPSK_P_2000_1.pdf
http://psasir.upm.edu.my/id/eprint/11267/
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spelling my.upm.eprints.112672024-06-13T06:17:57Z http://psasir.upm.edu.my/id/eprint/11267/ Congenital Kyphosis And Kyphoscoliosis: The Natural History And Results After Surgery Singh, Harwant Congenital kyphosis and kyphoscoliosis are due to vertebral anomalies that are present at birth. These vertebral anomalies cause a deformity of the spine in the sagittal plane. If allowed to progress, this deformity can produce neural dysfunction due to bowstringing of the cord over the apex of the deformity. The goals of this study were to document the natural history of congenital kyphosis and kyphoscoliosis and to determine the stage at which the natural history should be interrupted by treatment. This was done by reviewing the medical records and radiographs of the spine of 1 12 consecutive patients. Sixty eight patients had a type-I kyphosis due to anterior failure of vertebral-body formation, twentyfour had a type-II kyphosis due to anterior failure of vertebral-body segmentation, and twelve had a type-III kyphosis due to a combination of anomalies. The deformities of the remaining eight patients could not be classified. 2000-10 Thesis NonPeerReviewed text en http://psasir.upm.edu.my/id/eprint/11267/1/FPSK_P_2000_1.pdf Singh, Harwant (2000) Congenital Kyphosis And Kyphoscoliosis: The Natural History And Results After Surgery. Doctoral thesis, Universiti Putra Malaysia. English
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
English
description Congenital kyphosis and kyphoscoliosis are due to vertebral anomalies that are present at birth. These vertebral anomalies cause a deformity of the spine in the sagittal plane. If allowed to progress, this deformity can produce neural dysfunction due to bowstringing of the cord over the apex of the deformity. The goals of this study were to document the natural history of congenital kyphosis and kyphoscoliosis and to determine the stage at which the natural history should be interrupted by treatment. This was done by reviewing the medical records and radiographs of the spine of 1 12 consecutive patients. Sixty eight patients had a type-I kyphosis due to anterior failure of vertebral-body formation, twentyfour had a type-II kyphosis due to anterior failure of vertebral-body segmentation, and twelve had a type-III kyphosis due to a combination of anomalies. The deformities of the remaining eight patients could not be classified.
format Thesis
author Singh, Harwant
spellingShingle Singh, Harwant
Congenital Kyphosis And Kyphoscoliosis: The Natural History And Results After Surgery
author_facet Singh, Harwant
author_sort Singh, Harwant
title Congenital Kyphosis And Kyphoscoliosis: The Natural History And Results After Surgery
title_short Congenital Kyphosis And Kyphoscoliosis: The Natural History And Results After Surgery
title_full Congenital Kyphosis And Kyphoscoliosis: The Natural History And Results After Surgery
title_fullStr Congenital Kyphosis And Kyphoscoliosis: The Natural History And Results After Surgery
title_full_unstemmed Congenital Kyphosis And Kyphoscoliosis: The Natural History And Results After Surgery
title_sort congenital kyphosis and kyphoscoliosis: the natural history and results after surgery
publishDate 2000
url http://psasir.upm.edu.my/id/eprint/11267/1/FPSK_P_2000_1.pdf
http://psasir.upm.edu.my/id/eprint/11267/
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score 13.211869