MECP2 duplication syndrome: The electroclinical features of a case with long-term evolution

MECP2 duplication syndrome (MDS) is a rare and severe neurodevelopmental disorder frequently associated with epilepsy. Different seizure types and electroencephalographic (EEG) patterns were described in patients with MDS, although it lacks a specific phenotype.We report on an adult patient with lon...

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Bibliographic Details
Main Authors: Ilaria Cani, Lorenzo Muccioli, Francesco Mignani, Laura Licchetta, Paolo Tinuper, Federica Provini, Francesca Bisulli
Format: Article
Language:English
Published: Elsevier 2022-01-01
Series:Epilepsy & Behavior Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S2589986422000181

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