PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Phenotype | C0035372|rett syndrome |
| Sentences | 11 |
| PubMedID- 25346641 | What you seize is what you get: do we yet understand epilepsy in rett syndrome. |
| 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- 22476991 | An occurrence of epilepsy in rett syndrome is closely linked to early neurodevelopmental outcomes and poor functional abilities such as ambulation and hand use.11 we observed a tendency of lower ability of ambulation and poorer development in our epilepsy group than in our non-epilepsy group (table 1), though statistical correlation was not found in both aspects. |
| PubMedID- 20728410 | epilepsy in rett syndrome: clinical and genetic features. |
| PubMedID- 22998673 | epilepsy in rett syndrome, and cdkl5- and foxg1-gene-related encephalopathies. |
| 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- 25789914 | epilepsy in rett syndrome--lessons from the rett networked database. |
| PubMedID- 21764336 | epilepsy in rett syndrome: association between phenotype and genotype, and implications for practice. |
| 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. |
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