Introducing a Case of Aarskog-Scott Syndrome

dnshnmh Srm Pub Date : 2020-02-01 DOI:10.52547/sjrm.4.4.194
B. Bozorgmehr, Mohammad Reza Nateghi (MD, MPH), Dorin Tajbakhsh
{"title":"Introducing a Case of Aarskog-Scott Syndrome","authors":"B. Bozorgmehr, Mohammad Reza Nateghi (MD, MPH), Dorin Tajbakhsh","doi":"10.52547/sjrm.4.4.194","DOIUrl":null,"url":null,"abstract":"1 Sarem Fertility and Infertility Research Center (SAFIR), Sarem Women’s Hospital, Iran University of Medical Science (IUMS), Tehran, Iran 2 York University, Toronto, Canada Introduction: Aarskog-Scott syndrome is a rare X-linked disorder, charecterized by facial, skeletal and genital anomalies. It is also known as faciogenital dysplasia (FGDY, OMIM NO:305400) and facio-digito-genital syndrome. Patient Information: 7 years old boy with the same features, whom had been referred for genetic counseling, diagnosis, knowing the recurrence risk and seeking advice. Conclusion: The main features are short stature, hypertelorism, short hands and feet, and shawl scrotum.","PeriodicalId":33200,"journal":{"name":"dnshnmh Srm","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"dnshnmh Srm","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52547/sjrm.4.4.194","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

1 Sarem Fertility and Infertility Research Center (SAFIR), Sarem Women’s Hospital, Iran University of Medical Science (IUMS), Tehran, Iran 2 York University, Toronto, Canada Introduction: Aarskog-Scott syndrome is a rare X-linked disorder, charecterized by facial, skeletal and genital anomalies. It is also known as faciogenital dysplasia (FGDY, OMIM NO:305400) and facio-digito-genital syndrome. Patient Information: 7 years old boy with the same features, whom had been referred for genetic counseling, diagnosis, knowing the recurrence risk and seeking advice. Conclusion: The main features are short stature, hypertelorism, short hands and feet, and shawl scrotum.
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
介绍一例Aarskog-Scott综合征
1伊朗德黑兰伊朗医科大学萨雷姆妇女医院萨雷姆生育和不孕研究中心2加拿大多伦多约克大学简介:Aarskog-Scott综合征是一种罕见的X连锁疾病,表现为面部、骨骼和生殖器异常。它也被称为面生殖发育不良(FGDY,OMIM NO:305400)和面指生殖器综合征。患者信息:具有相同特征的7岁男孩,曾被转诊进行基因咨询、诊断、了解复发风险并寻求建议。结论:其主要特征为身材矮小、身高过大、手脚短、阴囊披肩。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
审稿时长
15 weeks
期刊最新文献
Vertical transmission of Covid-19 disease through umbilical cord blood: A cross-sectional study A case report of vague abdominal pain in the right lower quadrant (RLQ) and epigastric region: A mature cystic teratoma of the ovary Prenatal karyotype analysis of 8245 amniotic fluid samples of Iranian women and report of their chromosomal abnormalities: A 15-year single-center study A case report of a successful pregnancy with Budd-Chiari Syndrome Expression of ERBB1 gene in Iranian women with sporadic breast cancer and its relationship with clinicopathological features of the disease
×
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