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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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Bibliografiske detaljer
Principais autores: Helena F. Pernice, Susann May, Felix Mühlensiepen, Sebastian Spethmann, Ricarda Kneitz, Agata Mossakowski, Katrin Hahn
Format: Artigo
Sprog:Inglês
Udgivet: BMC 2026-02-01
Serier:Orphanet Journal of Rare Diseases
Fag:
Online adgang:https://doi.org/10.1186/s13023-026-04236-2
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