Rett syndrome: A rare case

Rett syndrome: A rare case

Rett syndrome (RTT) is rare, affects predominantly female children. It presents as a pervasive developmental disorder with a remarkable behavioral phenotype. The discovery that mutation in methyl-C-phosphate-G-binding protein 2 causes RTT has focused attention to the importance of epigenetic modific...

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Bibliographic Details
Main Authors: Deepika Verma, Daniel Saldanha, Aneek Saha, Kushagra Verma
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Medical Journal of Dr. D.Y. Patil University
Subjects:
Methyl-C-phosphate-G-binding protein 2
Rett syndrome
mental retardation
Online Access:http://www.mjdrdypu.org/article.asp?issn=0975-2870;year=2016;volume=9;issue=2;spage=241;epage=243;aulast=Verma

Internet

http://www.mjdrdypu.org/article.asp?issn=0975-2870;year=2016;volume=9;issue=2;spage=241;epage=243;aulast=Verma

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