Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Hereditary motor and sensory neuropathy type 6

MONDO:0019551

Also known as: CMT6, Charcot-Marie-Tooth disease type 6, hereditary motor and sensory neuropathy type 6, peripheral neuropathy and optic atrophy

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

Follow this condition — get notified about new trials

Sub-types

Neuropathy, hereditary motor and sensory, type 6A (0) Neuropathy, hereditary motor and sensory, type 6B (0) Neuropathy, hereditary motor and sensory, type VIc, with optic atrophy (0)

Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Peripheral nervous system disorder (114) Neuromuscular disease (106) Peripheral neuropathy (91) Human disease (14) Hereditary neurological disease (6) Hereditary peripheral neuropathy (6) Hereditary motor and sensory neuropathy (3)
Trials to join now! 5 Completed 1 Terminated 1
Sort by
  • 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

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space