• 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

Brief clinical report: 46,XX, del (18p) with amenorrhea, hypothyroidism, and ptosis.

作者信息

Stoffer S S, Koen A L, Abbasi A A, Brown S

出版信息

Am J Med Genet. 1981;9(4):285-90. doi: 10.1002/ajmg.1320090404.

DOI:10.1002/ajmg.1320090404
PMID:7294067
Abstract

A 17-year-old girl was initially evaluated because of primary amenorrhea and lack of sexual development. Chromosome studies demonstrated the presence of 46,XX, del (18p). The patient is now 21 years old and still has not menstruated. This is the first reported case of 46,XX, del (18p) presenting with primary amenorrhea. The case is of additional interest in that ptosis, a common finding in this syndrome, was not present at birth but was first noted at age 9.

摘要

相似文献

1
Brief clinical report: 46,XX, del (18p) with amenorrhea, hypothyroidism, and ptosis.
Am J Med Genet. 1981;9(4):285-90. doi: 10.1002/ajmg.1320090404.
2
Brief clinical report: Graves disease in a patient with the del(18p) syndrome.
Am J Med Genet. 1982 Apr;11(4):449-52. doi: 10.1002/ajmg.1320110410.
3
[Rare case of mosaicism for chromosome 18, karyotype: 46, XX, del(18) (p11)/46, XX, i(18q)].
Genetika. 1983 Nov;19(11):1912-5.
4
A triple-X female with long arm deletion of one of the X-chromosomes associated with primary amenorrhoea: 47,XX, +del(X) (q27.3).
Ann Genet. 1991;34(1):40-3.
5
[Deletion of the long arm of chromosome 18, primary hypothyroidism, Biermer's anemia and IgM hypogammaglobulinemia].[18号染色体长臂缺失、原发性甲状腺功能减退、比尔默贫血和IgM低丙种球蛋白血症]
Arch Fr Pediatr. 1989 Dec;46(10):729-32.
6
Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation.
Am J Med Genet. 1996 Aug 23;64(3):501-5. doi: 10.1002/(SICI)1096-8628(19960823)64:3<501::AID-AJMG11>3.0.CO;2-P.
7
Tetrasomy 18p: a distinctive syndrome.
Ann Genet. 1984;27(3):187-9.
8
Mosaic ring X chromosome in a case of secondary amenorrhea.一例继发性闭经患者的嵌合环形X染色体。
Fertil Steril. 2008 Oct;90(4):1198.e19-21. doi: 10.1016/j.fertnstert.2007.11.004. Epub 2008 Jan 4.
9
Primary amenorrhea and short arm deletion of the X chromosome, 46,X,del(Xp). Report of two cases.原发性闭经与X染色体短臂缺失,46,X,del(Xp)。两例报告。
N C Med J. 1982 Apr;43(4):287-8.
10
Cytogenetic studies in amenorrhea.闭经的细胞遗传学研究。
Saudi Med J. 2007 Feb;28(2):187-92.

引用本文的文献

1
Autoimmune thyroid disease and pituitary adenoma in a female patient with 18p deletion syndrome: a case report and review of the literature.一名患有18p缺失综合征女性患者的自身免疫性甲状腺疾病和垂体腺瘤:病例报告及文献复习
BMC Endocr Disord. 2025 Aug 25;25(1):199. doi: 10.1186/s12902-025-02017-9.
2
Heart disease associated with deletion of the short arm of chromosome 18.
Pediatr Cardiol. 1989 Summer;10(3):174-6. doi: 10.1007/BF02081684.