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Neuronopathy, distal hereditary motor, autosomal recessive 8

MONDO:0030055

Also known as: SORDD, sorbitol dehydrogenase deficiency, sorbitol dehydrogenase deficiency with peripheral neuropathy

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

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Broader categories

Disease (717) Nervous system disorder (243) Hereditary disease (188) Neurodegenerative disease (182) Peripheral nervous system disorder (119) Central nervous system disorder (115) Neuromuscular disease (110) Peripheral neuropathy (92) Motor neuron disorder (67) Human disease (15)

Trials to join now! 10 Not yet finished but already full! 4 Completed 2 Terminated 1

Could a simple blood test track nerve damage? a study investigates NT-3 levels in neuropathy.

Knowledge-focused Stopped early

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