First case report of Rett syndrome in the Azeri Turkish population and brief review of the literature

First case report of Rett syndrome in the Azeri Turkish population and brief review of the literature

Rett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the gene encoding methyl-CpG binding protein 2 (MECP2). Clinical manifestations include neurodevelopmental disorder characterized by early-onset intractable seizures, severe developmental delay, intellectual dis...

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Bibliographic Details
Main Authors: Jalal Gharesouran, Azizeh Farshbaf Khalili, Noushin Sorkhkoh Azari, Leila Vahedi
Format: Article
Language:English
Published: Elsevier 2015-01-01
Series:Epilepsy and Behavior Case Reports
Subjects:
Rett syndrome
MECP2 mutation
Azeri Turkish population
Online Access:http://www.sciencedirect.com/science/article/pii/S2213323214000541

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