Charcot-Marie-Tooth disease X-linked dominant 1

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Studying Nerve Function and Structure in Charcot-Marie-Tooth Disease, Anti-MAG Neuropathy and CIDP	Charcot-Marie-Tooth disease, Charcot-Marie-Tooth disease X-linked dominant 1, Charcot-Marie-Tooth disease type 1A, Charcot-Marie-Tooth disease type 4B2, Charcot-Marie-Tooth disease type 4D, Chronic Disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, autoimmune disease, autoimmune disorder of the nervous system, central nervous system malformation, chronic inflammatory demyelinating polyradiculoneuropathy, demyelinating disease, hereditary disease, hereditary motor and sensory neuropathy, immune system disorder, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG, polyradiculoneuropathy	Recruiting	Not stated	2026-03-10		NCT07461896

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