• 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

Kabuki make-up (Niikawa-Kuroki) syndrome: cognitive abilities and autistic features.

作者信息

Ho H H, Eaves L C

机构信息

University of British Columbia, Vancouver, Canada.

出版信息

Dev Med Child Neurol. 1997 Jul;39(7):487-90. doi: 10.1111/j.1469-8749.1997.tb07470.x.

DOI:10.1111/j.1469-8749.1997.tb07470.x
PMID:9285441
Abstract

Kabuki make-up syndrome (KMS), also known as Niikawa-Kuroki syndrome, is a rare malformation complex characterized by a peculiar facies with long palpebral fissures and partially everted lower eyelid, mental retardation, dwarfism, and skeletal and dermatoglyphic abnormalities. Four children from different ethnic groups presented with phenotypic manifestation of KMS. They showed variable degrees of learning disabilities, mental retardation, and autistic behavior. Two boys declined in IQ in early adolescence. In addition to being aware of the variable presentation of cognitive and behavioral characteristics in those already diagnosed, it is important to consider KMS when assessing dysmorphic children with learning disabilities and/or autism.

摘要

相似文献

1
Kabuki make-up (Niikawa-Kuroki) syndrome: cognitive abilities and autistic features.
Dev Med Child Neurol. 1997 Jul;39(7):487-90. doi: 10.1111/j.1469-8749.1997.tb07470.x.
2
The Niikawa-Kuroki (Kabuki make-up) syndrome in a Moslem Arab child.
Clin Genet. 1990 Nov;38(5):378-81. doi: 10.1111/j.1399-0004.1990.tb03599.x.
3
Kabuki makeup syndrome (Niikawa-Kuroki syndrome) in a black child.一名黑人儿童患歌舞伎综合征(丹川-黑木综合征)。
Ann Ophthalmol. 1989 Aug;21(8):312-5.
4
Niikawa-Kuroki (Kabuki) syndrome in two siblings.两名兄弟姐妹患有丹羽-黑木(歌舞伎)综合征。
Minerva Pediatr. 2001 Feb;53(1):43-8.
5
[Niikawa-Kuroki (Kabuki) syndrome and hearing impairment].[丹川-黑木(歌舞伎)综合征与听力障碍]
HNO. 2004 May;52(5):451-4. doi: 10.1007/s00106-003-0859-1.
6
Kabuki make-up syndrome (Niikawa-Kuroki syndrome) with cleft lip and palate.伴有唇腭裂的歌舞伎综合征(新川-黑木综合征)
J Craniomaxillofac Surg. 1991 Apr;19(3):99-101. doi: 10.1016/s1010-5182(05)80570-0.
7
Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients.歌舞伎综合征(丹川-黑木综合征):62例患者的研究
Am J Med Genet. 1988 Nov;31(3):565-89. doi: 10.1002/ajmg.1320310312.
8
The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients.歌舞伎(新川-黑木)综合征:29例非日本患者的表型进一步描述。
Eur J Pediatr. 1994 Jun;153(6):438-45. doi: 10.1007/BF01983409.
9
Niikawa-Kuroki syndrome.二川-黑木综合征
Minerva Pediatr. 1999 Jul-Aug;51(7-8):271-8.
10
Kabuki make-up syndrome with unilateral renal agenesis.
Turk J Pediatr. 2009 May-Jun;51(3):298-300.

引用本文的文献

1
From Genotype to Phenotype-A Review of Kabuki Syndrome.从基因型到表型——歌舞伎综合征综述。
Genes (Basel). 2022 Sep 29;13(10):1761. doi: 10.3390/genes13101761.
2
Dohsa-hou intervention for reciprocal interpersonal interaction for a girl with Kabuki syndrome and autism spectrum disorder.对一名患有歌舞伎综合征和自闭症谱系障碍的女孩进行土佐法互惠人际互动干预。
Clin Case Rep. 2021 Jun 24;9(6):e04296. doi: 10.1002/ccr3.4296. eCollection 2021 Jun.
3
Neurobehavioral features in individuals with Kabuki syndrome.歌舞伎综合征患者的神经行为特征。
Mol Genet Genomic Med. 2018 May;6(3):322-331. doi: 10.1002/mgg3.348. Epub 2018 Mar 13.
4
A Child with Kabuki Syndrome and Autism Spectrum Disorder.一名患有歌舞伎综合征和自闭症谱系障碍的儿童。
Noro Psikiyatr Ars. 2016 Sep;53(3):280-282. doi: 10.5152/npa.2015.10099. Epub 2016 Sep 1.
5
De novo mutations in genes of mediator complex causing syndromic intellectual disability: mediatorpathy or transcriptomopathy?中介体复合物基因的新生突变导致综合征性智力障碍:中介体病还是转录组病?
Pediatr Res. 2016 Dec;80(6):809-815. doi: 10.1038/pr.2016.162. Epub 2016 Aug 8.
6
Kabuki syndrome: clinical and molecular characteristics.歌舞伎综合征:临床与分子特征
Korean J Pediatr. 2015 Sep;58(9):317-24. doi: 10.3345/kjp.2015.58.9.317. Epub 2015 Sep 21.
7
A mutation screen in patients with Kabuki syndrome.卡布奇诺综合征患者的突变筛查。
Hum Genet. 2011 Dec;130(6):715-24. doi: 10.1007/s00439-011-1004-y. Epub 2011 May 24.
8
Case report: autistic disorder in Kabuki syndrome.病例报告:歌舞伎综合征中的自闭症谱系障碍
J Autism Dev Disord. 2008 Jan;38(1):198-201. doi: 10.1007/s10803-007-0433-x. Epub 2007 Aug 25.