Rett Syndrome (RTT, MIM 312750), a progressive neurodevelopmental disease, has an approximately incidence rate of 1 in 10,000 (Neul et al., 2010) in live female births. RTT becomes visible through a neurodevelopmental regression following 6 to 18 months apparent normal developmental period. Loss of acquired language skills, stereotypic hand movements, and comprehensive cognitive, social, motor skill