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Distal hereditary motor neuropathy type 7

MONDO:0015355

Distal hereditary motor neuropathy type 7 is a rare, slowly progressive genetic peripheral neuropathy characterized by distal atrophy and weakness affecting the upper limbs (with a predilection for the thenar eminence) and subsequently the lower limbs, associated with uni- or bilateral vocal cord paresis leading to hoarse voice and breathing difficulties, and facial weakness.

Also known as: dHMN7, distal spinal muscular atrophy with vocal cord paralysis

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

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Sub-types

Neuronopathy, distal hereditary motor, type 7A (0) Neuronopathy, distal hereditary motor, type 7B (0)

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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