New dysostosis showing multilevel absence of vertebral pedicles: unique developmental anomaly of vertebral arches?

American Journal of Medical Genetics Pub Date : 2000-12-18
A Verloes, C Muller, P Philippet
{"title":"New dysostosis showing multilevel absence of vertebral pedicles: unique developmental anomaly of vertebral arches?","authors":"A Verloes,&nbsp;C Muller,&nbsp;P Philippet","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We report on an apparently normal child who shows hypopaplasia of the vertebral pedicles and posterior arches of several cervical, thoracic, and lumbar vertebrae with normally fused spinous apophyses, hypoplastic sacrum, lumbar epidural lipomatosis, synostoses of some cervical vertebral disks, and sacral spina bifida. The most likely mechanism is an abnormal differentiation of the spinal processes, due most probably to an absence of differentiation in cartilage of the dense mesenchyme forming their most anterior part. Because the anomalies affect multiple levels, we highly suspect a genetic basis to this unusual dysostosis affecting the development of the posterior sclerotomes.</p>","PeriodicalId":7708,"journal":{"name":"American Journal of Medical Genetics","volume":"95 5","pages":"473-6"},"PeriodicalIF":0.0000,"publicationDate":"2000-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Medical Genetics","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

We report on an apparently normal child who shows hypopaplasia of the vertebral pedicles and posterior arches of several cervical, thoracic, and lumbar vertebrae with normally fused spinous apophyses, hypoplastic sacrum, lumbar epidural lipomatosis, synostoses of some cervical vertebral disks, and sacral spina bifida. The most likely mechanism is an abnormal differentiation of the spinal processes, due most probably to an absence of differentiation in cartilage of the dense mesenchyme forming their most anterior part. Because the anomalies affect multiple levels, we highly suspect a genetic basis to this unusual dysostosis affecting the development of the posterior sclerotomes.

多节段椎弓根缺失:椎弓发育异常?
我们报告了一个表面上正常的儿童,他表现出椎弓根发育不全和几个颈椎、胸椎和腰椎的后弓发育不全,并伴有正常融合的棘突,骶骨发育不全,腰椎硬膜外脂肪增生,一些颈椎椎间盘滑脱,以及骶骨脊柱裂。最可能的机制是脊柱突的异常分化,很可能是由于形成其最前部的致密间质软骨缺乏分化。由于异常影响多个水平,我们高度怀疑这种不寻常的骨缺损影响后巩膜发育的遗传基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信