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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

15 clinical trials for this condition and its sub-types, 0 tagged with Distal hereditary motor neuropathy type 7 itself.

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↑ Neuronopathy, distal hereditary motor, autosomal dominant (0)

Sub-types of Distal hereditary motor neuropathy type 7

Neuronopathy, distal hereditary motor, type 7A 0 trials
Neuronopathy, distal hereditary motor, type 7B 0 trials

Including sub-types (15) Tagged with Distal hereditary motor neuropathy type 7 (0)

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