Abstract
Charcot-Marie-Tooth (CMT) disease is the most common inherited neuromuscular disorder, with variable age of onset (from infancy to adulthood) and a broad phenotypic spectrum. Several motor function and disability scales in CMT patients are available. The aim of this study is to better characterize CMT in its forms, also providing a clinical follow-up tool.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
