• 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

[Dysgenesis of CNS in dyscranio-pygo-phalangia (author's transl)].

作者信息

Hori A, Murofushi K, Iizuka R

出版信息

Acta Neuropathol. 1976 Aug 16;35(4):327-32.

PMID:822683
Abstract

A rare case of dyscranio-pygo-phalangia was studied neuropathologically. The patient was a 19 days old boy, who showed multiple anomalies: protuberance of forehead, narrow eye fissures, microphthalmos, micrognathia, microauriculae with dysplasia, hexadactylia of extremities, cryptorchism, asymmetric thorax, congenital heart disease and hypoplasia of the right lung. There were multiple dysgeneses in the central nervous system, especially the cerebellum: floccular heterotopia; heterotopias of cortex type, cerebellar nucleic type and Purkinje cell type; external granular layer cells in the white matter; dentate spindle-cell-dysgenesis. Other findings were glio-neurono-mesenchymal dysgenesis on the surface of the brain, residual fetal external granular layer on the surface of the pons, partial hypoplasia of corpus callosum, heterotopic nerve cells in the molecular layer of the periinsular cortex.

摘要

相似文献

1
[Dysgenesis of CNS in dyscranio-pygo-phalangia (author's transl)].
Acta Neuropathol. 1976 Aug 16;35(4):327-32.
2
Brain dysgenesis in Cornelia de Lange syndrome.
Clin Neuropathol. 1999 Mar-Apr;18(2):99-105.
3
Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.里彻-申策尔颅-小脑-心脏(3C)综合征:4例新病例报告及文献复习
Am J Med Genet. 2001 Aug 15;102(3):237-42.
4
Patient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts.
Am J Med Genet. 2002 May 1;109(3):206-10. doi: 10.1002/ajmg.10283.
5
Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome).肢端肥大性额鼻“发育异常”:对一种伴有脑畸形和多指畸形(托列洛综合征)的亚型的进一步描述
Am J Med Genet. 1992 Jan 15;42(2):180-3. doi: 10.1002/ajmg.1320420209.
6
Aplasia cutis congenita associated with limb, eye, and brain anomalies in sibs: a variant of the Adams-Oliver syndrome?同胞中先天性皮肤发育不全合并肢体、眼部及脑部异常:亚当斯-奥利弗综合征的一种变异型?
Am J Med Genet. 1995 Oct 23;59(1):92-5. doi: 10.1002/ajmg.1320590118.
7
[Ullrich-Feichtiger syndrome in a 3-year-old boy].[一名3岁男孩的乌利希-费希蒂格综合征]
Pol Tyg Lek. 1992;47(9-10):234-5.
8
[Associated brain anomalies and clinical findings in corpus callosum dysgenesis].胼胝体发育不全相关的脑异常及临床发现
Tani Girisim Radyol. 2003 Dec;9(4):411-7.
9
Cerebral abnormalities in the Neu-Laxova syndrome.
Am J Med Genet. 1988 Jul;30(3):747-56. doi: 10.1002/ajmg.1320300308.
10
Cerebello-cortical heterotopia in dentate nucleus, and other microdysgeneses in trisomy D1 (Patau) syndrome.
Brain Dev. 1980;2(4):345-52.