Volume 4, Issue 4 (2020)
SJMR 2020, 4(4): 194-197 |
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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
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
2- York University, Toronto, Canada
Abstract: (3333 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.
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.
Article Type: Case Report |
Subject:
Sterility Genetical Disorders
Received: 2020/05/31 | Accepted: 2020/10/20 | Published: 2020/12/19
Received: 2020/05/31 | Accepted: 2020/10/20 | Published: 2020/12/19
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