Charcot-Marie-Tooth disease neuronal type B
Other Names for this Disease
- Charcot Marie Tooth disease neuronal type B
These Web pages are updated as the Genetic and Rare Diseases Information Center receives questions and as new information becomes available. If you don’t see many information resources on this page, it may be because the Information Center hasn’t yet received a question about this condition.
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Please contact us with your questions about Charcot-Marie-Tooth disease neuronal type B. We will answer your question and update these pages with new resources and information.
On this page
- The Muscular Dystrophy Association has developed an information page entitled "Surgery Sometimes, Bracing Often, Caution Always: Caring for the CMT-affected Foot." Click on Muscular Dystrophy Association to view this information page.