Autosomal dominant Charcot-Marie-Tooth disease type 2I
Synonyms: CMT2I
A form of axonal Charcot-Marie-Tooth disease a peripheral sensorimotor neuropathy characterized by a late onset with severe sensory loss (paresthesia and hypoesthesia) associated with distal weakness mainly of the legs and absent or reduced deep tendon reflexes.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Autosomal dominant Charcot-Marie-Tooth disease type 2I?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Advocacy Organizations
Charcot-Marie-Tooth Association
To develop drugs to treat or cure CMT and to help improve the quality of life for those living with CMT.
Clinical Trials
For a list of clinical trials in this disease area, please click here.