Volume 4, Issue 4 (2020)                   SJMR 2020, 4(4): 194-197 | Back to browse issues page

Research code: ندارد
Ethics code: ندارد
Clinical trials code: ندارد

XML Persian Abstract Print

Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Bozorgmehr B, Nateghi M R, Tajbakhsh D. Introducing a Case of Aarskog-Scott Syndrome. SJMR. 2020; 4 (4) :194-197
URL: http://saremjrm.com/article-1-171-en.html
1- Sarem Fertility and Infertility Research Center (SAFIR), Sarem Women’s Hospital, Iran University of Medical Sciences (IUMS), Tehran, Iran
2- York University, Toronto, Canada
Abstract:   (1219 Views)
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.
Full-Text [PDF 645 kb]   (509 Downloads)    
Article Type: Case Report | Subject: Sterility Genetical Disorders
Received: 2020/05/31 | Accepted: 2020/10/20 | Published: 2020/12/19

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2022 CC BY-NC 4.0 | {Sarem Journal of Medical Research}

Designed & Developed by : Yektaweb