Cardiac autonomic control in Rett syndrome: Insights from heart rate variability analysis

Cardiac autonomic control in Rett syndrome: Insights from heart rate variability analysis

Rett syndrome (RTT) is a rare and severe neurological disorder mainly affecting females, usually linked to methyl-CpG-binding protein 2 (MECP2) gene mutations. Manifestations of RTT typically include loss of purposeful hand skills, gait and motor abnormalities, loss of spoken language, stereotypic h...

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Bibliographic Details
Main Authors: Ramona Cordani, Eleonora Tobaldini, Gabriel Dias Rodrigues, Donatella Giambersio, Marco Veneruso, Lorenzo Chiarella, Nicola Disma, Elisa De Grandis, Edgar Toschi-Dias, Ludovico Furlan, Angelica Carandina, Giulia Prato, Lino Nobili, Nicola Montano
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-03-01
Series:Frontiers in Neuroscience
Subjects:
Rett syndrome (RTT)
dysautonomia
methyl-CpG-binding protein 2 (MECP2)
cardiac autonomic control
autonomic nervous system
heart rate variability (HRV)
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2023.1048278/full

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https://www.frontiersin.org/articles/10.3389/fnins.2023.1048278/full

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