Paradoxical physiological responses to propranolol in a Rett syndrome patient: a case report

BACKGROUND: Rett Syndrome (RTT), caused by a loss-of-function in the epigenetic modulator: X-linked methyl-CpG binding protein 2 (MeCP2), is a pervasive neurological disorder characterized by compromised brain functions, anxiety, severe mental retardation, language and learning disabilities, repetit...

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Detalles Bibliográficos
Autores principales: Santosh, P. J., Bell, L., Lievesley, K., Singh, J., Fiori, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129599/
https://www.ncbi.nlm.nih.gov/pubmed/27899087
http://dx.doi.org/10.1186/s12887-016-0734-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129599/
https://www.ncbi.nlm.nih.gov/pubmed/27899087
http://dx.doi.org/10.1186/s12887-016-0734-3

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