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- W2921117830 abstract "Rett Syndrome (RTT) is a genetic neurodevelopmental disorder characterized by normal early development followed by loss of purposeful use of the hands and of muscle tone, and acquisition of distinctive hand movements, slowed brain and head growth, gait abnormalities, seizures, and intellectual disability. It almost exclusively affects females. Another symptom, apraxia — the inability to perform motor functions — is perhaps the most severely disabling feature of RTT, interfering with every body movement, including eye gaze and speech." @default.
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- W2921117830 date "2019-03-01" @default.
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- W2921117830 title "Attention measures of patients with Rett Syndrome need to overcome the challenges in evaluating the oculomotor function using electronystagmography" @default.
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- W2921117830 doi "https://doi.org/10.1016/j.ejpn.2019.02.008" @default.
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