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Cites:

Information Journal Paper

Title

Introducing a Case of Aarskog-Scott Syndrome (Case Report)

Pages

  194-197

Abstract

 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.

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  • Cite

    APA: Copy

    BOZORGMEHR, BITA, NATEGHI, MOHAMMAD REZA, & Tajbakhsh, Dorin. (2020). Introducing a Case of Aarskog-Scott Syndrome (Case Report). SAREM JOURNAL OF MEDICAL RESEARCH (SAREM JOURNAL OF REPRODUCTIVE MEDICINE), 4(4 ), 194-197. SID. https://sid.ir/paper/383865/en

    Vancouver: Copy

    BOZORGMEHR BITA, NATEGHI MOHAMMAD REZA, Tajbakhsh Dorin. Introducing a Case of Aarskog-Scott Syndrome (Case Report). SAREM JOURNAL OF MEDICAL RESEARCH (SAREM JOURNAL OF REPRODUCTIVE MEDICINE)[Internet]. 2020;4(4 ):194-197. Available from: https://sid.ir/paper/383865/en

    IEEE: Copy

    BITA BOZORGMEHR, MOHAMMAD REZA NATEGHI, and Dorin Tajbakhsh, “Introducing a Case of Aarskog-Scott Syndrome (Case Report),” SAREM JOURNAL OF MEDICAL RESEARCH (SAREM JOURNAL OF REPRODUCTIVE MEDICINE), vol. 4, no. 4 , pp. 194–197, 2020, [Online]. Available: https://sid.ir/paper/383865/en

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