• 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

Váradi syndrome (OFD VI) or Opitz trigonocephaly syndrome: overlapping manifestations in two cousins.

作者信息

Cleper R, Kauschansky A, Varsano I, Frydman M

机构信息

Department of Pediatrics, Hasharon Hospital, Petah Tiqwa, Israel.

出版信息

Am J Med Genet. 1993 Sep 15;47(4):451-5. doi: 10.1002/ajmg.1320470402.

DOI:10.1002/ajmg.1320470402
PMID:8256802
Abstract

We report on 2 cousins, offspring of consanguineous matings, with multiple congenital anomalies. Square face, frontal bossing with metopic ridge, small anteverted nose, flat nasal bridge, slanted palpebral fissures, and epicanthal folds contributed to an unusual appearance. Multiple bucco-alveolar frenula and notched inferior alveolar ridges were present at birth and one had a notched uvula and submucous cleft of the hard palate. Both had congenital heart anomalies, micropenis, and cryptorchidism. Persistence of Müllerian structures was documented at necropsy in one patient. The surviving patient was mentally retarded and had unilateral central hexadactyly and partial agenesis of the corpus callosum. Bulimia and episodic hyperthermia were attributed to hypothalamic dysfunction. Results of unstimulated endocrine studies and gonadotropin releasing hormone (GnRH), and human chorionic gonadotropin (HCG) stimulation tests were normal. The manifestations of the 2 patients overlap those reported in the OFD VI and Opitz trigonocephaly syndromes.

摘要

相似文献

1
Váradi syndrome (OFD VI) or Opitz trigonocephaly syndrome: overlapping manifestations in two cousins.
Am J Med Genet. 1993 Sep 15;47(4):451-5. doi: 10.1002/ajmg.1320470402.
2
Varadi syndrome or Opitz trigonocephaly: overlapping manifestation in two cousins.
Am J Med Genet. 1994 Oct 15;53(1):85-8. doi: 10.1002/ajmg.1320530119.
3
Opitz trigonocephaly syndrome.
Am J Med Genet. 1991 Sep 15;40(4):444-6. doi: 10.1002/ajmg.1320400413.
4
[Opitz-trigonocephaly syndrome--a characteristic dysmorphia-retardation syndrome of unclear origin].[奥匹茨三角头畸形综合征——一种起源不明的典型畸形-智力发育迟缓综合征]
Klin Padiatr. 1992 May-Jun;204(3):171-3. doi: 10.1055/s-2007-1025345.
5
A new X-linked multiple congenital anomalies/mental retardation syndrome.一种新的X连锁多发性先天性畸形/智力发育迟缓综合征。
Am J Med Genet. 1984 Jan;17(1):367-74. doi: 10.1002/ajmg.1320170130.
6
Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.智力发育迟缓、先天性心脏缺陷、腭裂、身材矮小及面部异常:一种新的X连锁多发性先天性异常/智力发育迟缓综合征:临床描述与分子研究
Am J Med Genet. 1994 Jul 15;51(4):591-7. doi: 10.1002/ajmg.1320510459.
7
Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.
Am J Med Genet. 1995 Nov 20;59(3):329-33. doi: 10.1002/ajmg.1320590310.
8
Further delineation of the C (trigonocephaly) syndrome.C(三角头畸形)综合征的进一步描述。
Am J Med Genet. 1981;9(2):147-63. doi: 10.1002/ajmg.1320090209.
9
Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality.史密斯-勒米-奥皮茨综合征II型:伴有男性假两性畸形和频繁早期致死率的多种先天性异常。
Am J Med Genet. 1987 Jan;26(1):45-57. doi: 10.1002/ajmg.1320260110.
10
Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children.
Am J Med Genet. 1995 Nov 20;59(3):276-82. doi: 10.1002/ajmg.1320590303.

引用本文的文献

1
Clinical and molecular heterogeneity of syndromic hypothalamic hamartoma.综合征性下丘脑错构瘤的临床和分子异质性。
Am J Med Genet A. 2023 Sep;191(9):2337-2343. doi: 10.1002/ajmg.a.63306. Epub 2023 Jul 12.
2
Stringent delineation of Pallister-Hall syndrome in two long surviving patients: importance of radiological anomalies of the hands.两名长期存活患者中帕利斯特-霍尔综合征的严格界定:手部放射学异常的重要性
J Med Genet. 1995 Aug;32(8):605-11. doi: 10.1136/jmg.32.8.605.