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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主要な著者:	Helena F. Pernice, Susann May, Felix Mühlensiepen, Sebastian Spethmann, Ricarda Kneitz, Agata Mossakowski, Katrin Hahn
フォーマット:	Artigo
言語:	Inglês
出版事項:	BMC 2026-02-01
シリーズ:	Orphanet Journal of Rare Diseases
主題:	Patient journey CMT Hereditary neuropathy Healthcare Survey
オンライン･アクセス:	https://doi.org/10.1186/s13023-026-04236-2
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