Wikisage, the free encyclopedia of the second generation, is digital heritage
Rett syndrome: Difference between revisions
Jump to navigation
Jump to search
m (rfz) |
(cat) |
||
| Line 10: | Line 10: | ||
<references/> | <references/> | ||
[[Category:Medicine]] | |||
Revision as of 18:05, 31 July 2015
The syndrome was first described by Andreas Rett in 1966. Since the discovery of mutations in the methyl-CpG binding protein-2 (MECP2) gene in Rett Syndrome (RTT) a large number of females have been diagnosed worldwide [1]
epilepsy, includying status epilepticus [2][3][4]
Disease classification WHO
F84.2 Rett syndrome
- ↑ Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients
- ↑ http://www.apsu.org.au/assets/workshops/rett/Rett-syndrome-epilepsy.pdf
- ↑ Epilepsy and the natural history of Rett syndrome
- ↑ Epilepsy in Rett syndrome: Association between phenotype and genotype, and implications for practice