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Charcot-Marie-Tooth disease type 2B1

MONDO:0011569

Charcot-Marie-Tooth disease, type 2B1 (CMT2B1, also referred to as CMT4C1) is an axonal CMT peripheral sensorimotor polyneuropathy.

Also known as: AR-CMT2B1, CMT2B1, Charcot-Marie-Tooth disease type 2 caused by mutation in LMNA, Charcot-Marie-Tooth disease, type 2B1, LMNA Charcot-Marie-Tooth disease type 2, autosomal recessive Charcot-Marie-Tooth disease type 2B1, autosomal recessive axonal CMT4C1, CMT 2B1

10 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Peripheral nervous system disorder (114) Neuromuscular disease (106) Peripheral neuropathy (91) Charcot-Marie-Tooth disease (48) Human disease (14) Hereditary neurological disease (6) Hereditary peripheral neuropathy (6)
Trials to join now! 8 Completed 1 Terminated 1
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  • Could a simple blood test track nerve damage? a study investigates NT-3 levels in neuropathy.

    Knowledge-focused Terminated

    This study measures levels of a protein called NT-3 in the blood of people with peripheral neuropathy or Charcot-Marie-Tooth disease. Researchers will compare these levels with measures of muscle strength, mobility, and daily function. The goal is to see whether NT-3 levels corre…

    Sponsor: Zarife Sahenk • Aim: Knowledge-focused

    Last updated Jul 31, 2026 00:00 UTC

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