Sleep Disorders in Rett Syndrome and Rett-Related Disorders: A Narrative Review

Rett Syndrome (RTT) is a rare and severe X-linked developmental brain disorder that occurs primarily in females, with a ratio of 1:10.000. De novo mutations in the Methyl-CpG Binding protein 2 (MECP2) gene on the long arm of X chromosome are responsible for more than 95% cases of classical Rett. In...

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Detalles Bibliográficos
Autores principales: Tascini, Giorgia, Dell'Isola, Giovanni Battista, Mencaroni, Elisabetta, Di Cara, Giuseppe, Striano, Pasquale, Verrotti, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923297/
https://www.ncbi.nlm.nih.gov/pubmed/35299616
http://dx.doi.org/10.3389/fneur.2022.817195

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923297/
https://www.ncbi.nlm.nih.gov/pubmed/35299616
http://dx.doi.org/10.3389/fneur.2022.817195

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