• 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

身材矮小及一种有趣的关联。

Short stature and an interesting association.

作者信息

Sneha Latha Magatha, Thanasegarapandian Kishore, Paramasivam Venkataraman, Scott Julius Xavier

机构信息

Department of Pediatrics, Sri Ramachandra University, Chennai, Tamil Nadu, India.

出版信息

Indian J Hum Genet. 2013 Jan;19(1):101-3. doi: 10.4103/0971-6866.112919.

DOI:10.4103/0971-6866.112919
PMID:23901203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3722618/
Abstract

Untreated hypothyroidism in children usually results in delayed puberty, but juvenile hypothyroidism causes isosexual precocious puberty in a rare syndrome called Van Wyk Grumbach syndrome, with a complete reversal to the pre pubertal state following thyroid hormone replacement therapy. We report here, a 7-year-old girl who presented with short stature, constipation and isosexual precocious puberty due to the long standing untreated severe hypothyroidism with this syndrome.

摘要

儿童未经治疗的甲状腺功能减退通常会导致青春期延迟,但青少年甲状腺功能减退在一种罕见的综合征——范怀克-格伦巴赫综合征中会导致同性性早熟,甲状腺激素替代治疗后会完全恢复到青春期前状态。我们在此报告一名7岁女孩,她因长期未经治疗的严重甲状腺功能减退伴该综合征而出现身材矮小、便秘和同性性早熟。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c8/3722618/1d34a898a7a9/IJHG-19-101-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c8/3722618/edfd3216a11a/IJHG-19-101-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c8/3722618/1d34a898a7a9/IJHG-19-101-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c8/3722618/edfd3216a11a/IJHG-19-101-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c8/3722618/1d34a898a7a9/IJHG-19-101-g002.jpg

相似文献

1
Short stature and an interesting association.身材矮小及一种有趣的关联。
Indian J Hum Genet. 2013 Jan;19(1):101-3. doi: 10.4103/0971-6866.112919.
2
Van Wyk-Grumbach syndrome and oligosyndactyly in a 6-year-old girl: a case report.一名6岁女孩的范·怀克-格伦巴赫综合征与少指(趾)畸形:病例报告
J Med Case Rep. 2020 Sep 16;14(1):166. doi: 10.1186/s13256-020-02472-z.
3
Van Wyk-Grumbach syndrome with hemangioma in an infant.一名患有血管瘤的婴儿的范·怀克-格伦巴赫综合征。
J Pediatr Endocrinol Metab. 2018 Sep 25;31(9):1057-1060. doi: 10.1515/jpem-2018-0049.
4
Van Wyk Grumbach Syndrome: A Rare Consequence of Hypothyroidism.范维克-格鲁姆巴赫综合征:甲状腺功能减退症的罕见后果。
Indian J Pediatr. 2018 Nov;85(11):1028-1030. doi: 10.1007/s12098-018-2704-2. Epub 2018 May 19.
5
Van Wyk-Grumbach Syndrome with Kocher-Debré-Sémélaigne Syndrome: Case Report of a Rare Association.范·怀克-格伦巴赫综合征合并科赫尔-德布勒-塞梅拉涅综合征:罕见关联病例报告
Eur Thyroid J. 2017 Feb;6(1):47-51. doi: 10.1159/000448993. Epub 2016 Oct 4.
6
Imaging in Van Wyk Grumbach syndrome: An uncommon presentation of hypothyroidism.范·怀克-格鲁巴赫综合征的影像学表现:一种罕见的甲状腺功能减退症表现。
SA J Radiol. 2023 Mar 15;27(1):2572. doi: 10.4102/sajr.v27i1.2572. eCollection 2023.
7
Van Wyk-Grumbach syndrome: The importance of thyroid function tests in a child presenting with multicystic ovaries.范·怀克-格鲁姆巴赫综合征:甲状腺功能检查在患有多囊卵巢的儿童中的重要性。
Int J Surg Case Rep. 2024 Jan;114:109097. doi: 10.1016/j.ijscr.2023.109097. Epub 2023 Nov 28.
8
An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism.一名患有范维克-格伦巴赫综合征的奥尔波特综合征男孩,由长期未治疗的先天性甲状腺功能减退症诱发。
Ann Pediatr Endocrinol Metab. 2020 Jun;25(2):132-136. doi: 10.6065/apem.1938074.037. Epub 2020 Jun 30.
9
Van Wyk-Grumbach syndrome in a female pediatric patient with trisomy 21: a case report.一名患有21三体综合征的女性儿科患者的范·怀克-格伦巴赫综合征:病例报告
Int J Pediatr Endocrinol. 2020;2020:2. doi: 10.1186/s13633-020-0072-y. Epub 2020 Jan 28.
10
Van Wyk-Grumbach Syndrome and Gonadectomy.范·怀克-格鲁姆巴赫综合征与性腺切除术
Children (Basel). 2024 Jul 8;11(7):831. doi: 10.3390/children11070831.

引用本文的文献

1
Van Wyk-Grumbach Syndrome and Gonadectomy.范·怀克-格鲁姆巴赫综合征与性腺切除术
Children (Basel). 2024 Jul 8;11(7):831. doi: 10.3390/children11070831.
2
The Clinical Septet of Van Wyk-Grumbach Syndrome: A Case Series from a Tertiary Care Centre in Kalyana Karnataka, India.范·怀克-格伦巴赫综合征的临床七联征:来自印度卡利亚纳卡纳塔克邦一家三级医疗中心的病例系列
touchREV Endocrinol. 2023 May;19(1):98-102. doi: 10.17925/EE.2023.19.1.98. Epub 2023 Feb 6.
3
Delayed Diagnosis of Hypothyroidism in Children: Report of 3 Cases.儿童甲状腺功能减退症的延迟诊断:3例报告

本文引用的文献

1
Van Wyk and Grumbach Syndrome (A Syndrome of Incomplete Isosexual Precocity and Juvenile Hypothyroidism).范·怀克和格鲁巴赫综合征(一种不完全同性性早熟和青少年甲状腺功能减退综合征)。
Med J Armed Forces India. 2002 Oct;58(4):343-5. doi: 10.1016/S0377-1237(02)80095-8. Epub 2011 Jul 21.
2
An unusual presentation of a usual disorder: Van Wyk-Grumbach syndrome.一种常见病症的不寻常表现:范·怀克 - 格伦巴赫综合征。
Indian J Endocrinol Metab. 2011 Jul;15(Suppl 2):S141-3. doi: 10.4103/2230-8210.83356.
3
CASE OF PRECOCIOUS PUBERTY IN A FEMALE CRETIN.
Iran Red Crescent Med J. 2015 Nov 1;17(11):e20306. doi: 10.5812/ircmj.20306. eCollection 2015 Nov.
一例女性克汀病患者的性早熟病例
Br Med J. 1905 Feb 4;1(2301):246. doi: 10.1136/bmj.1.2301.246.
4
A case of multiple ovarian cysts in a prepubertal girl with severe hypothyroidism due to autoimmune thyroiditis.一名青春期前女孩因自身免疫性甲状腺炎导致严重甲状腺功能减退,并发多发性卵巢囊肿的病例。
Int J Gynecol Cancer. 2004 May-Jun;14(3):543-5. doi: 10.1111/j.1048-891x.2004.14318.x.
5
Polycystic ovaries, precocious puberty and acquired hypothyroidism: The Van Wyk and Grumbach syndrome.多囊卵巢、性早熟和获得性甲状腺功能减退:范怀克和格伦巴赫综合征。
J Pediatr Surg. 2003 Sep;38(9):1390-2. doi: 10.1016/s0022-3468(03)00403-2.
6
Primary hypothyroidism and ovarian activity evidence for an overlap in the synthesis of pituitary glycoproteins. Case report.原发性甲状腺功能减退与卵巢活动:垂体糖蛋白合成重叠的证据。病例报告。
Br J Obstet Gynaecol. 1981 Feb;88(2):195-202. doi: 10.1111/j.1471-0528.1981.tb00967.x.
7
Thyroid disease and reproductive dysfunction: a review.甲状腺疾病与生殖功能障碍:综述
Obstet Gynecol. 1987 Nov;70(5):789-98.
8
Plasma prolactin and thyrotropin and the response to thyrotropin-releasing factor in children with primary and hypothalamic hypothyroidism.原发性和下丘脑性甲状腺功能减退患儿的血浆催乳素、促甲状腺激素及对促甲状腺激素释放因子的反应
J Clin Endocrinol Metab. 1978 Nov;47(5):1015-20. doi: 10.1210/jcem-47-5-1015.