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Neuronopathy, distal hereditary motor, type 2A

MONDO:0008025

Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB8 gene. The presenting symptoms are paresis of the extensor muscles of the big toe and later of the extensor muscles of the feet and chronic neurogenic alterations in electromyography.

Also known as: HSPB8 neuronopathy, distal hereditary motor, neuronopathy, distal hereditary motor caused by mutation in HSPB8, HMN2A, neuronopathy, distal hereditary motor, type IIA

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

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodegenerative disease (155) Peripheral nervous system disorder (107) Neuromuscular disease (98) Central nervous system disorder (97) Spinal muscular atrophy (93) Peripheral neuropathy (90) Motor neuron disorder (59)
Trials to join now! 18 Not yet recruiting 2 Not yet finished but already full! 3 Completed 6
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