Rett Syndrome (RTT) is a neurodevelopmental disorder caused by mutations of the MECP2 gene, affecting predominantly females. One of the characteristic features of the disease is defective brainstem autonomic function. In Mecp2 mice, several groups of brainstem neurons are overly excitable, which causes destabilization of neuronal networks for the autonomic control.
View Article and Find Full Text PDFBackground: Rett syndrome (RTT) is a neurodevelopmental disorder caused mostly by disruptions in the gene. -null mice show imbalances in neuronal excitability and synaptic communications. Several previous studies indicate that augmenting synaptic GABA receptors (GABARs) can alleviate RTT-like symptoms in mice.
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