Patient journey with Charcot-Marie-Tooth Disease – A German patient survey study
Abstract Background Charcot-Marie-Tooth (CMT) and related disorders represent one of the largest groups of inherited neurological disorders. Long considered incurable, the first disease-modifying treatments are currently being evaluated in clinical trials. However, frequent misdiagnosis or delayed r...
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| Autori principali: | , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMC
2026-02-01
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| Serie: | Orphanet Journal of Rare Diseases |
| Soggetti: | |
| Accesso online: | https://doi.org/10.1186/s13023-026-04236-2 |
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