兄弟姐妹中Duane异常、先天性肌病和严重脊柱侧凸:新的AR综合征?

Alain Verloes , Jean-Paul Misson , Philippe Gillet , Clarisse Baumann , Micheline Spiritus , Manuel Deprez
{"title":"兄弟姐妹中Duane异常、先天性肌病和严重脊柱侧凸:新的AR综合征?","authors":"Alain Verloes ,&nbsp;Jean-Paul Misson ,&nbsp;Philippe Gillet ,&nbsp;Clarisse Baumann ,&nbsp;Micheline Spiritus ,&nbsp;Manuel Deprez","doi":"10.1016/S0003-3995(03)00018-2","DOIUrl":null,"url":null,"abstract":"<div><p>We report on two sisters who show a similar pattern of anomalies consisting of bilateral Stilling–Türk–Duane retraction syndrome (type 3), non-progressive hypotonia with delayed motor milestones but normal intelligence, severe, early onset scoliosis, and short stature. Muscular biopsy revealed numerous regenerating fibers, but no specific abnormalities among the non-regenerating fibers. This combination of anomalies has not been previously reported, and could represent a new autosomal recessive syndrome. The only differential diagnosis is Crisfield–Dretakis–Sharpe syndrome, a combination of lateral gaze palsy, ptosis, and scoliosis without hypotonia, recessively inherited.</p></div>","PeriodicalId":100089,"journal":{"name":"Annales de Génétique","volume":"46 4","pages":"Pages 449-452"},"PeriodicalIF":0.0000,"publicationDate":"2003-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0003-3995(03)00018-2","citationCount":"0","resultStr":"{\"title\":\"Duane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome?\",\"authors\":\"Alain Verloes ,&nbsp;Jean-Paul Misson ,&nbsp;Philippe Gillet ,&nbsp;Clarisse Baumann ,&nbsp;Micheline Spiritus ,&nbsp;Manuel Deprez\",\"doi\":\"10.1016/S0003-3995(03)00018-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We report on two sisters who show a similar pattern of anomalies consisting of bilateral Stilling–Türk–Duane retraction syndrome (type 3), non-progressive hypotonia with delayed motor milestones but normal intelligence, severe, early onset scoliosis, and short stature. Muscular biopsy revealed numerous regenerating fibers, but no specific abnormalities among the non-regenerating fibers. This combination of anomalies has not been previously reported, and could represent a new autosomal recessive syndrome. The only differential diagnosis is Crisfield–Dretakis–Sharpe syndrome, a combination of lateral gaze palsy, ptosis, and scoliosis without hypotonia, recessively inherited.</p></div>\",\"PeriodicalId\":100089,\"journal\":{\"name\":\"Annales de Génétique\",\"volume\":\"46 4\",\"pages\":\"Pages 449-452\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0003-3995(03)00018-2\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annales de Génétique\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0003399503000182\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annales de Génétique","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0003399503000182","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

我们报告了两名姐妹,她们表现出类似的异常模式,包括双侧stillling - t rk - duane后缩综合征(3型),非进行性张力低下伴运动里程碑延迟,但智力正常,严重的早发性脊柱侧凸和身材矮小。肌肉活检显示大量再生纤维,但非再生纤维未见特殊异常。这种异常的组合以前没有报道过,可能代表一种新的常染色体隐性综合征。唯一的鉴别诊断是Crisfield-Dretakis-Sharpe综合征,这是一种隐性遗传的组合,包括侧视麻痹、上睑下垂和脊柱侧凸,但无强直。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Duane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome?

We report on two sisters who show a similar pattern of anomalies consisting of bilateral Stilling–Türk–Duane retraction syndrome (type 3), non-progressive hypotonia with delayed motor milestones but normal intelligence, severe, early onset scoliosis, and short stature. Muscular biopsy revealed numerous regenerating fibers, but no specific abnormalities among the non-regenerating fibers. This combination of anomalies has not been previously reported, and could represent a new autosomal recessive syndrome. The only differential diagnosis is Crisfield–Dretakis–Sharpe syndrome, a combination of lateral gaze palsy, ptosis, and scoliosis without hypotonia, recessively inherited.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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