Autosomal dominant Charcot-Marie-Tooth disease type 2D

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Autosomal dominant Charcot-Marie-Tooth disease type 2D

Synonyms: CMT2D

A form of axonal Charcot-Marie-Tooth disease a peripheral sensorimotor neuropathy characterized by distal weakness primarily and predominantly occurring in the upper limbs and tendon reflexes absent or reduced in the arms and decreased in the legs. Progression is slow.

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 March 2024

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Autosomal dominant Charcot-Marie-Tooth disease type 2D?

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Clinical Trials

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