Characteristics of adult individuals with Rett syndrome treated or untreated with trofinetide in the United States
BackgroundRett syndrome (RTT) is a rare, progressive MECP2-related neurodevelopmental disorder with substantial lifelong morbidity that persists into adulthood. Although survival has improved, adults often experience evolving multisystem complications and fragmented transition care. Trofinetide (TRO...
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| Hoofdauteurs: | , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
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Frontiers Media S.A.
2026-07-01
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| Reeks: | Frontiers in Neurology |
| Onderwerpen: | |
| Online toegang: | https://www.frontiersin.org/articles/10.3389/fneur.2026.1856312/full |
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