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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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| Publicado no: | Orphanet J Rare Dis |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4832563/ https://ncbi.nlm.nih.gov/pubmed/27080038 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0418-y |
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