eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | rett syndrome |
| Symptom | C0014544|epilepsy |
| Sentences | 10 |
| PubMedID- 22946725 | They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the pcdh 19 gene. |
| PubMedID- 25789914 | epilepsy in rett syndrome--lessons from the rett networked database. |
| PubMedID- 22998673 | epilepsy in rett syndrome, and cdkl5- and foxg1-gene-related encephalopathies. |
| PubMedID- 20728410 | epilepsy in rett syndrome: clinical and genetic features. |
| PubMedID- 20491871 | epilepsy in rett syndrome---the experience of a national rett center. |
| PubMedID- 26089674 | Management of epilepsy in patients with rett syndrome: perspectives and considerations. |
| PubMedID- 23583050 | Our goal in this review is to better define the clinical and electrophysiological aspects of the epilepsy associated with rett syndrome and provide practical guidance regarding management. |
| PubMedID- 21764336 | epilepsy in rett syndrome: association between phenotype and genotype, and implications for practice. |
| PubMedID- 23421866 | Aim: the aim of this study was to identify characteristics of epilepsy in rett syndrome (rtt), and relationships between epilepsy and genotype. |
| PubMedID- 25346641 | What you seize is what you get: do we yet understand epilepsy in rett syndrome. |
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