IGSF1缺乏综合征:一种新发现的内分泌疾病。

Rare diseases (Austin, Tex.) Pub Date : 2013-05-02 eCollection Date: 2013-01-01 DOI:10.4161/rdis.24883
Sjoerd D Joustra, A S Paul van Trotsenburg, Yu Sun, Monique Losekoot, Daniel J Bernard, Nienke R Biermasz, Wilma Oostdijk, Jan M Wit
{"title":"IGSF1缺乏综合征:一种新发现的内分泌疾病。","authors":"Sjoerd D Joustra,&nbsp;A S Paul van Trotsenburg,&nbsp;Yu Sun,&nbsp;Monique Losekoot,&nbsp;Daniel J Bernard,&nbsp;Nienke R Biermasz,&nbsp;Wilma Oostdijk,&nbsp;Jan M Wit","doi":"10.4161/rdis.24883","DOIUrl":null,"url":null,"abstract":"<p><p>A recently uncovered X-linked syndrome, caused by loss-of-function of IGSF1, is characterized by congenital central hypothyroidism and macroorchidism, variable prolactin deficiency, occasional growth hormone deficiency, delayed pubertal testosterone secretion and obesity. We propose to call this endocrinopathy \"IGSF1 deficiency syndrome.\" Based on an estimated incidence of isolated congenital central hypothyroidism of 1:65,000, we predict that the incidence of IGSF1 deficiency related hypothyroidism is approximately 1:100,000. IGSF1 encodes a plasma membrane immunoglobulin superfamily glycoprotein that is highly expressed in pituitary and testis, but is of unknown function. The variable profile of pituitary dysfunction suggests that IGSF1 may play a role in pituitary paracrine regulation. The clinical significance of the syndrome, particularly the clinical consequences of untreated hypothyroidism, justifies screening family members of patients with IGSF1 mutations for carriership and to study potential carriers of IGSF1 mutations, including patients with idiopathic central hypothyroidism, combined GH and TSH deficiency, macroorchidism or delayed puberty. </p>","PeriodicalId":74639,"journal":{"name":"Rare diseases (Austin, Tex.)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2013-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4161/rdis.24883","citationCount":"17","resultStr":"{\"title\":\"IGSF1 deficiency syndrome: A newly uncovered endocrinopathy.\",\"authors\":\"Sjoerd D Joustra,&nbsp;A S Paul van Trotsenburg,&nbsp;Yu Sun,&nbsp;Monique Losekoot,&nbsp;Daniel J Bernard,&nbsp;Nienke R Biermasz,&nbsp;Wilma Oostdijk,&nbsp;Jan M Wit\",\"doi\":\"10.4161/rdis.24883\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A recently uncovered X-linked syndrome, caused by loss-of-function of IGSF1, is characterized by congenital central hypothyroidism and macroorchidism, variable prolactin deficiency, occasional growth hormone deficiency, delayed pubertal testosterone secretion and obesity. We propose to call this endocrinopathy \\\"IGSF1 deficiency syndrome.\\\" Based on an estimated incidence of isolated congenital central hypothyroidism of 1:65,000, we predict that the incidence of IGSF1 deficiency related hypothyroidism is approximately 1:100,000. IGSF1 encodes a plasma membrane immunoglobulin superfamily glycoprotein that is highly expressed in pituitary and testis, but is of unknown function. The variable profile of pituitary dysfunction suggests that IGSF1 may play a role in pituitary paracrine regulation. The clinical significance of the syndrome, particularly the clinical consequences of untreated hypothyroidism, justifies screening family members of patients with IGSF1 mutations for carriership and to study potential carriers of IGSF1 mutations, including patients with idiopathic central hypothyroidism, combined GH and TSH deficiency, macroorchidism or delayed puberty. </p>\",\"PeriodicalId\":74639,\"journal\":{\"name\":\"Rare diseases (Austin, Tex.)\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-05-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.4161/rdis.24883\",\"citationCount\":\"17\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Rare diseases (Austin, Tex.)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4161/rdis.24883\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2013/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rare diseases (Austin, Tex.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4161/rdis.24883","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 17

摘要

最近发现的一种由IGSF1功能丧失引起的x连锁综合征,其特征是先天性中枢性甲状腺功能减退和巨睾酮功能亢进、变异性催乳素缺乏、偶发性生长激素缺乏、青春期睾酮分泌延迟和肥胖。我们建议将这种内分泌疾病称为“IGSF1缺乏综合征”。根据孤立性先天性中枢性甲状腺功能减退症的估计发病率为1:6万5千,我们预测IGSF1缺乏相关甲状腺功能减退症的发病率约为1:10万。IGSF1编码一种质膜免疫球蛋白超家族糖蛋白,在垂体和睾丸中高度表达,但功能未知。垂体功能障碍的不同特征表明IGSF1可能在垂体旁分泌调节中发挥作用。该综合征的临床意义,特别是未经治疗的甲状腺功能减退的临床后果,证明了对IGSF1突变患者的家庭成员进行携带者筛查,并研究IGSF1突变的潜在携带者,包括特发性中枢性甲状腺功能减退、GH和TSH合并缺乏症、大睾丸功能亢进或青春期延迟的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
IGSF1 deficiency syndrome: A newly uncovered endocrinopathy.

A recently uncovered X-linked syndrome, caused by loss-of-function of IGSF1, is characterized by congenital central hypothyroidism and macroorchidism, variable prolactin deficiency, occasional growth hormone deficiency, delayed pubertal testosterone secretion and obesity. We propose to call this endocrinopathy "IGSF1 deficiency syndrome." Based on an estimated incidence of isolated congenital central hypothyroidism of 1:65,000, we predict that the incidence of IGSF1 deficiency related hypothyroidism is approximately 1:100,000. IGSF1 encodes a plasma membrane immunoglobulin superfamily glycoprotein that is highly expressed in pituitary and testis, but is of unknown function. The variable profile of pituitary dysfunction suggests that IGSF1 may play a role in pituitary paracrine regulation. The clinical significance of the syndrome, particularly the clinical consequences of untreated hypothyroidism, justifies screening family members of patients with IGSF1 mutations for carriership and to study potential carriers of IGSF1 mutations, including patients with idiopathic central hypothyroidism, combined GH and TSH deficiency, macroorchidism or delayed puberty.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Primary Immunodeficiency Chronic Myeloid Leukemia Milestone Histories and Paradigmatic Genetic Discoveries of Chronic Myeloid Leukemia (CML) Duchenne Muscular Dystrophy (DMD) Diagnosis: Past and Present Perspectives Rare Disease Advocacy Groups and Their Significance in Diagnosis, Management, Treatment, and Prevention of Rare Diseases
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1