• 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

Craniofrontonasal dysplasia in two male sibs.

作者信息

Natarajan U, Baraitser M, Nicolaides K, Gosden C

机构信息

Mothercare Unit of Clinical Genetics, Institute of Child Health, London, UK.

出版信息

Clin Dysmorphol. 1993 Oct;2(4):360-4.

PMID:8305967
Abstract

Craniofrontonasal dysplasia (CFND) was diagnosed in a male child who had bilateral coronal craniosynostosis, midline facial clefting with cleft lip and palate, a broad and high forehead, and hypertelorism. The parents were normal and there was no family history suggestive of CFND. A small recurrence risk was counselled and prenatal ultrasound was recommended in the next pregnancy. At 23 weeks, the ultrasound scan detected a number of dysmorphic features and the pregnancy was terminated. Autopsy of the aborted male foetus showed the following features: High arched palate, a sloping forehead, flattened nose and receding chin, multiple joint contractures, particularly of the mid phalangeal joints, elbows and ankles. This report highlights the occurrence of CFND in two male siblings born to normal parents, and therefore the need to perform prenatal ultrasound in a subsequent pregnancy, even if CFND is diagnosed in an isolated case.

摘要

相似文献

1
Craniofrontonasal dysplasia in two male sibs.
Clin Dysmorphol. 1993 Oct;2(4):360-4.
2
Craniofrontonasal dysplasia: more severe expression in the mother than in her son.
Genet Couns. 1995;6(4):361-4.
3
Oto-palato-digital syndrome type II.II型耳-腭-指综合征
Genet Couns. 1994;5(1):61-6.
4
Craniofrontonasal dysplasia.
Eur J Pediatr. 1992 Nov;151(11):837-41. doi: 10.1007/BF01957936.
5
[Prenatal diagnosis of skeletal dysplasia: case report of a fetus with multiple anomalies].[骨骼发育不良的产前诊断:一例多发畸形胎儿的病例报告]
Med Pregl. 2000 Mar-Apr;53(3-4):197-201.
6
[Robinow's syndrome associated with deafness].[与耳聋相关的罗宾诺综合征]
Arch Fr Pediatr. 1993 Dec;50(10):897-9.
7
New autosomal dominant syndrome resembling craniofrontonasal dysplasia.
Am J Med Genet. 1987 Nov;28(3):581-91. doi: 10.1002/ajmg.1320280306.
8
Acalvaria, holoprosencephaly, and facial dysmorphism syndrome.
J Craniofac Genet Dev Biol Suppl. 1986;2:319-29.
9
Oto-palato-digital syndrome with features of type I and II in brothers.
Genet Couns. 1995;6(3):233-40.
10
G syndrome: an unusual family.
Am J Med Genet. 1988 Nov;31(3):637-42. doi: 10.1002/ajmg.1320310319.

引用本文的文献

1
Isolated Sagittal Synostosis in a Boy with Craniofrontonasal Dysplasia and a Novel EFNB1 Mutation.一名患有颅额鼻发育不良及新型EFNB1突变男孩的孤立性矢状缝早闭
Plast Reconstr Surg Glob Open. 2015 Jul 8;3(6):e427. doi: 10.1097/GOX.0000000000000369. eCollection 2015 Jun.
2
Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1.EFNB1基因致病性突变患者的颅额鼻综合征表型
Eur J Hum Genet. 2014 Aug;22(8):995-1001. doi: 10.1038/ejhg.2013.273. Epub 2013 Nov 27.
3
The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males.
颅额鼻综合征中EFNB1突变的起源:频繁的体细胞镶嵌现象及男性携带者稀少的原因
Am J Hum Genet. 2006 Jun;78(6):999-1010. doi: 10.1086/504440. Epub 2006 Apr 28.