Prevalence and onset of comorbidities in the CDKL5 disorder differ from Rett syndrome

BACKGROUND: Initially described as an early onset seizure variant of Rett syndrome, the CDKL5 disorder is now considered as an independent entity. However, little is currently known about the full spectrum of comorbidities that affect these patients and available literature is limited to small case...

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Detalles Bibliográficos
Autores principales: Mangatt, Meghana, Wong, Kingsley, Anderson, Barbara, Epstein, Amy, Hodgetts, Stuart, Leonard, Helen, Downs, Jenny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832563/
https://www.ncbi.nlm.nih.gov/pubmed/27080038
http://dx.doi.org/10.1186/s13023-016-0418-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832563/
https://www.ncbi.nlm.nih.gov/pubmed/27080038
http://dx.doi.org/10.1186/s13023-016-0418-y

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