How I treat Rett syndrome: impact of trofinetide on symptoms and comorbidities of the disease
Rett syndrome (RTT) is a rare neurodevelopmental disorder primarily associated with mutations in the MECP2 gene that lead to developmental regression and difficulties with language, motor skills, and hand use. Additionally, patients with RTT suffer from seizures, scoliosis, issues with sleep, and be...
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| Formaat: | Artigo |
| Taal: | Inglês |
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Taylor & Francis Group
2026-12-01
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| Reeks: | Future Rare Diseases |
| Onderwerpen: | |
| Online toegang: | https://www.tandfonline.com/doi/10.1080/23995270.2026.2705911 |
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