• 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

Focal dermal hypoplasia syndrome. An update.

作者信息

Goltz R W

出版信息

Arch Dermatol. 1992 Aug;128(8):1108-11.

PMID:1497368
Abstract
摘要

相似文献

1
Focal dermal hypoplasia syndrome. An update.局灶性真皮发育不全综合征。最新进展。
Arch Dermatol. 1992 Aug;128(8):1108-11.
2
Myelomeningocele, Arnold-Chiari anomaly and hydrocephalus in focal dermal hypoplasia.局灶性真皮发育不全中的脊髓脊膜膨出、阿诺德-奇亚里畸形和脑积水。
Am J Med Genet. 1988 Aug;30(4):917-23. doi: 10.1002/ajmg.1320300407.
3
Focal dermal hypoplasia (Goltz-Gorlin syndrome).局灶性真皮发育不全(戈尔茨-戈林综合征)。
Quintessence Int. 2002 Oct;33(9):706-7.
4
A family presenting Goltz syndrome (focal dermal hypoplasia) in three generations.一个三代人都患有戈尔茨综合征(局灶性真皮发育不全)的家族。
Turk J Pediatr. 1998 Oct-Dec;40(4):593-601.
5
Three cases of focal dermal hypoplasia (Goltz syndrome).三例局灶性真皮发育不全(戈尔茨综合征)。
Clin Exp Dermatol. 2005 Jan;30(1):35-7. doi: 10.1111/j.1365-2230.2004.01647.x.
6
Focal dermal hypoplasia with unusual cutaneous features.
Pediatr Dermatol. 2007 Jul-Aug;24(4):387-90. doi: 10.1111/j.1525-1470.2007.00455.x.
7
[Focal dermal hypoplasia (Goltz's syndrome). Review of the literature and clinical contribution].
Minerva Stomatol. 1989 Apr;38(4):439-43.
8
Case of unilateral focal dermal hypoplasia (Goltz syndrome).单侧局限性皮肤发育不全(戈尔茨综合征)病例。
J Dermatol. 2008 Jan;35(1):33-5. doi: 10.1111/j.1346-8138.2007.00408.x.
9
Airway management in a patient with focal dermal hypoplasia.
Anesth Analg. 2006 Nov;103(5):1342. doi: 10.1213/01.ane.0000242323.73548.0b.
10
Focal dermal hypoplasia (Goltz-Gorlin syndrome) associated with obstructive papillomatosis of the larynx and hypopharynx.
Eur J Dermatol. 1999 Dec;9(8):618-20.

引用本文的文献

1
[Focal dermal hypoplasia associated with pathogenic PORCN gene variant in postzygotic, unilateral mosaic form].[与致病性PORCN基因变异相关的局限性皮肤发育不全,呈合子后单侧镶嵌形式]
Dermatologie (Heidelb). 2024 Jun;75(6):486-491. doi: 10.1007/s00105-024-05308-9. Epub 2024 Feb 16.
2
Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia.患有局灶性真皮发育不全的儿童和成人的皮肤、颅骨及骨骼缺陷
Children (Basel). 2023 Oct 22;10(10):1715. doi: 10.3390/children10101715.
3
Focal Dermal Hypoplasia: Case Series.
局灶性真皮发育不全:病例系列
Indian J Dermatol. 2023 Jan-Feb;68(1):122. doi: 10.4103/ijd.ijd_508_22.
4
Life-long Skin Eruptions along Blaschko's Lines in a 27-year-old Woman: A Quiz.一名27岁女性沿布拉斯科线出现的终身性皮肤疹:一则病例问答
Acta Derm Venereol. 2021 Dec 7;101(12):adv00610. doi: 10.2340/actadv.v101.193.
5
A Rare Case of Mainly Unilateral Focal Dermal Hypoplasia (Goltz Syndrome) in an Adult Male: A Case Report and Review of the Literature.成年男性主要表现为单侧局灶性皮肤发育不全(戈尔茨综合征)的罕见病例:病例报告及文献综述
J Med Cases. 2020 Mar;11(3):61-64. doi: 10.14740/jmc3442. Epub 2020 Mar 26.
6
Hair follicle stem cells as a skin-organizing signaling center during adult homeostasis.毛囊干细胞作为成体稳态期间皮肤组织的信号中心。
EMBO J. 2021 Jun 1;40(11):e107135. doi: 10.15252/embj.2020107135. Epub 2021 Apr 20.
7
and Mutations in a Highly Consanguineous Family.并在一个高度近亲结婚的家族中发现了突变。
Int J Mol Sci. 2021 Feb 4;22(4):1549. doi: 10.3390/ijms22041549.
8
The Genetic Architecture of High Bone Mass.高骨量的遗传结构。
Front Endocrinol (Lausanne). 2020 Oct 29;11:595653. doi: 10.3389/fendo.2020.595653. eCollection 2020.
9
Stromal Vascular Fraction and its Role in the Management of Alopecia: A Review.基质血管成分及其在脱发管理中的作用:综述
J Clin Aesthet Dermatol. 2019 Nov;12(11):35-44. Epub 2019 Nov 1.
10
A Rare Case of Squamous Cell Carcinoma of the Esophagus in a Patient With Goltz Syndrome.戈茨综合征患者发生食管鳞状细胞癌的罕见病例。
ACG Case Rep J. 2019 Mar 8;6(3):1-4. doi: 10.14309/crj.0000000000000045. eCollection 2019 Mar.