0897 Sleep Architecture and Epileptiform Discharges in Rett Syndrome
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DOI: 10.1093/sleep/zsad077.0897
Abstract: Rett syndrome (RTT) is an X-linked dominant neurodevelopmental disorder affecting females and is linked to mutations in the methyl-CpG-binding protein 2 (MeCP2) gene. Sleep issues and frequent epileptiform discharges are common in RTT. Typical comorbidities… read more here.
Keywords: epileptiform discharges; 0897 sleep; rett syndrome; rtt patients ... See more keywords
Changes in the Cerebrospinal Fluid and Plasma Lipidome in Patients with Rett Syndrome
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DOI: 10.3390/metabo12040291
Abstract: Rett syndrome (RTT) is defined as a rare disease caused by mutations of the methyl-CpG binding protein 2 (MECP2). It is one of the most common causes of genetic mental retardation in girls, characterized by… read more here.
Keywords: rett syndrome; cerebrospinal fluid; plasma; rtt patients ... See more keywords