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| ICD-10 | ||
|---|---|---|
| ICD-9 | ||
| OMIM | [1] | |
| DiseasesDB | [2] | |
| MedlinePlus | [3] | |
| eMedicine | neuro/468 | |
| MeSH | {{{MeshNumber}}} | |
Hereditary motor and sensory neuropathies (HMSN) are a group of neuropathies which are characterized by their impact upon both afferent and efferent neural communication.
They are more common than hereditary sensory and autonomic neuropathies.[1]
Types[]
In 1968, it was classified from groups I to VII:[2][3]
| Type | Name | Diseases Database | OMIM |
| I | Charcot-Marie-Tooth disease 1 | 5815 | 118220, 118200 |
| II | Charcot-Marie-Tooth disease 2 | 2343 | 118210, 600882 |
| III | Dejerine Sottas syndrome | 5821 | 145900 |
| IV | Refsum's disease | 11213 | 266500 |
| V | HMSN+hereditary spastic paraplegia | - | 600361 |
| VI | HMSN+hereditary optic atrophy | 32095 | 601152 |
| VII | HMSN+retinitis pigmentosa | 32094 | - |
HMSN is sometimes equated with Charcot-Marie-Tooth disease.[4][5]
See also[]
References[]
- ↑ Houlden H, Blake J, Reilly MM (October 2004). Hereditary sensory neuropathies. Curr. Opin. Neurol. 17 (5): 569–77.
- ↑ eMedicine - Charcot-Marie-Tooth and Other Hereditary Motor and Sensory Neuropathies : Article by Aamir Hashmat.
- ↑ Dyck PJ, Lambert EH (June 1968). Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. Arch. Neurol. 18 (6): 603–18.
- ↑ Horacek O, Mazanec R, Morris CE, Kobesova A (October 2007). Spinal deformities in hereditary motor and sensory neuropathy: a retrospective qualitative, quantitative, genotypical, and familial analysis of 175 patients. Spine 32 (22): 2502–8.
- ↑ Bertorini T, Narayanaswami P, Rashed H (November 2004). Charcot-Marie-Tooth disease (hereditary motor sensory neuropathies) and hereditary sensory and autonomic neuropathies. Neurologist 10 (6): 327–37.
Further reading[]
- Reilly MM (October 2000). Classification of the hereditary motor and sensory neuropathies. Curr. Opin. Neurol. 13 (5): 561–4.
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