A Case Report of Fragile X Syndrome with Fingers Anomaly

A Case Report of Fragile X Syndrome with Fingers Anomaly

Fragile X Syndrome, the most common cause of inherited mental retardation, results from mutation in fragile X mental retardation gene (FMR1) on long arm of X chromosome, Xq27.3. Clinical features include moderate to severe mental retardation without neurologic deficit, long face, large ears, promine...

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Bibliographic Details
Main Authors: Farah Ashrafzadeh, Mohammad Reza Abbaszadegan, Nosrat Ghaemi
Format: Article
Language:fas
Published: Hamadan University of Medical Sciences 2003-06-01
Series:پزشکی بالینی ابن سینا
Subjects:
fragile x syndrome
gene fmr 1
macroorchidism
mental retardation
Online Access:http://sjh.umsha.ac.ir/article-1-690-en.html

Internet

http://sjh.umsha.ac.ir/article-1-690-en.html

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