Hereditary motor and sensory neuropathy

MONDO:0015358

A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-Tooth DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)

Also known as: HMSN

9 clinical trials for this condition and its sub-types, 3 tagged with Hereditary motor and sensory neuropathy itself.

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↑ Hereditary peripheral neuropathy (478)

Sub-types of Hereditary motor and sensory neuropathy

Autosomal dominant slowed nerve conduction velocity 0 trials
Demyelinating hereditary motor and sensory neuropathy 0 trials
Hereditary motor and sensory neuropathy type 6 0 trials
3 sub-types
Hereditary motor and sensory neuropathy with acrodystrophy 0 trials
Hereditary sensorimotor neuropathy with hyperelastic skin 0 trials
Hereditary thermosensitive neuropathy 0 trials
Polyneuropathy-hand defect syndrome 0 trials
Severe early-onset axonal neuropathy due to MFN2 deficiency 0 trials

Including sub-types (9) Tagged with Hereditary motor and sensory neuropathy (3)

Trials to join now! 2 Not yet finished but already full! 1

Hereditary motor and sensory neuropathy

Where it sits in the disease tree

Massive CMT study aims to map disease progression over five years

Scientists hunt for hidden genes behind nerve disease severity