• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Fetal akinesia-hypokinesia deformation sequence (FADS) in 2 siblings with congenital myotonic dystrophy.

作者信息

Lidang Jensen M, Rix M, Schroder H D, Teglbjaerg P S, Ebbesen F

机构信息

Department of Pathology, Odense Hospital, Denmark.

出版信息

Clin Neuropathol. 1995 Mar-Apr;14(2):105-8.

PMID:7606895
Abstract

Two premature siblings described herein had clinical features comparable to the fetal akinesia-hypokinesia deformation sequence (Pena-Shokeir syndrome) with polyhydramnios, intrauterine growth retardation, pulmonary hypoplasia, short umbilical cord and lethality. Autopsy revealed no thoracal or abdominal viscera anomalies and examination of the brain, spinal cord and peripheral nerves did not disclose any pathological changes. Light microscopy, immunohistochemistry and electron microscopy of skeletal muscles demonstrated immature muscles with some fibril disorganisation and abnormal immunoreactivity for actin and desmin. Subsequent molecular genetic analysis revealed a maternal diagnosis of myotonic dystrophy. The retarded growth and maturation of skeletal muscle observed in the presented cases correspond with previous findings in neonatal myotonic dystrophy. A well-defined myopathy can thus result in the fetal akinesia-hypokinesia deformation sequence.

摘要

相似文献

1
Fetal akinesia-hypokinesia deformation sequence (FADS) in 2 siblings with congenital myotonic dystrophy.
Clin Neuropathol. 1995 Mar-Apr;14(2):105-8.
2
Incidence of fetal akinesia-hypokinesia deformation sequence: a population-based study.
Acta Paediatr. 2009 Jan;98(1):3-4. doi: 10.1111/j.1651-2227.2008.01102.x.
3
Analysis of Pena Shokeir phenotype.佩纳-绍凯尔综合征表型分析
Am J Med Genet. 1986 Sep;25(1):99-117. doi: 10.1002/ajmg.1320250112.
4
[Foetal akinesia-hypokinesia deformation sequence].[胎儿运动减少-运动不能性变形序列征]
Ugeskr Laeger. 2010 May 10;172(19):1457-9.
5
[Familial akinesia-hypokinesia sequence (Pena-Shokier phenotype)].[家族性运动不能-运动减少序列征(佩纳-肖基尔表型)]
Geburtshilfe Frauenheilkd. 1994 May;54(5):276-85. doi: 10.1055/s-2007-1022840.
6
[Genetic-morphologic fatal syndromes. Fetal akinesia sequence (Pena-Shokeir syndrome I)].[遗传形态学致死综合征。胎儿运动不能序列征(佩纳-绍凯尔综合征I型)]
Pathologe. 1993 Jul;14(4):216-8.
7
An autopsy case of Pena-Shokeir syndrome: severe retardation of skeletal muscle development compared with neuronal abnormalities.一例佩纳-肖克综合征尸检病例:与神经元异常相比,骨骼肌发育严重迟缓。
Pediatr Pathol Mol Med. 2002 Sep-Oct;21(5):467-76. doi: 10.1080/15227950290104797.
8
[Pena-Shokeir syndrome: report of a case with benign outcome].
Pediatr Med Chir. 1995 Jan-Feb;17(1):73-5.
9
Heterogeneity in fetal akinesia deformation sequence (FADS): autopsy confirmation in three 20-21-week fetuses.胎儿运动不能变形序列征(FADS)的异质性:3例20 - 21周胎儿的尸检证实
Prenat Diagn. 2002 Jan;22(1):42-7. doi: 10.1002/pd.234.
10
[Role of signs of fetal hypokinesia in the diagnosis of spinal muscular atrophy of neonatal onset].[胎儿运动减少体征在新生儿期起病的脊髓性肌萎缩症诊断中的作用]
An Esp Pediatr. 2002 Mar;56(3):233-40.

引用本文的文献

1
Human brain pathology in myotonic dystrophy type 1: A systematic review.1 型肌强直性营养不良的人脑病理学:系统评价。
Neuropathology. 2021 Feb;41(1):3-20. doi: 10.1111/neup.12721.
2
Pena-Shokeir syndrome: current management strategies and palliative care.佩纳-肖克综合征:当前的管理策略与姑息治疗
Appl Clin Genet. 2018 Oct 25;11:111-120. doi: 10.2147/TACG.S154643. eCollection 2018.