Rett syndrome: a review of clinical manifestations and therapeutic approaches
Rett syndrome (RTT) is a severe X-linked dominant neurodevelopmental disorder predominantly affecting females and over 90% of these patients mutations linked to the methyl-CpG-binding protein 2 (MeCP2) gene. Although the syndrome is well noted for the classic repetitive hand motion with decline in s...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2024-05-01
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| Serie: | Frontiers in Sleep |
| Soggetti: | |
| Accesso online: | https://www.frontiersin.org/articles/10.3389/frsle.2024.1373489/full |
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