Ad blocker interference detected!
Wikia is a free-to-use site that makes money from advertising. We have a modified experience for viewers using ad blockers
Wikia is not accessible if you’ve made further modifications. Remove the custom ad blocker rule(s) and the page will load as expected.
Individual differences |
Methods | Statistics | Clinical | Educational | Industrial | Professional items | World psychology |
Hereditary motor and sensory neuropathies (HMSN) are a group of neuropathies which are characterized by their impact upon both afferent and efferent neural communication.
|Type||Other names||Diseases Database||OMIM|
|HMSN1||Charcot–Marie–Tooth disease type 1||5815||(multiple)|
|HMSN2||Charcot–Marie–Tooth disease type 2||2343||(multiple)|
|HMSN3|| Dejerine–Sottas disease|
Charcot–Marie–Tooth disease type 3
|HMSN5|| Charcot–Marie–Tooth disease with pyramidal features|
HMSN with pyramidal features
|HMSN6|| Charcot–Marie–Tooth disease type 6|
HMSN with optic atrophy
- Charcot–Marie–Tooth disease
- Hereditary motor neuropathies
- Hereditary sensory and autonomic neuropathies
- Spinal muscular atrophies
- ↑ 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.
- ↑ DOI:10.1097/BRS.0b013e3181573d4e
- ↑ DOI:10.1097/01.nrl.0000145596.38640.27
- Reilly MM (October 2000). Classification of the hereditary motor and sensory neuropathies. Curr. Opin. Neurol. 13 (5): 561–4.
Nervous system pathology, primarily PNS (G50-G99, 350-359)
|Nerve, nerve root|
and plexus disorders
cranial nerve: V (Trigeminal neuralgia) - VII (Facial nerve paralysis, Bell's palsy, Melkersson-Rosenthal syndrome, Central seven) - XI (Accessory nerve disorder)
and other disorders of the PNS
| Diseases of myoneural junction|
Myasthenia gravis - Primary disorders of muscles (Muscular dystrophy, Myotonic dystrophy, Myotonia congenita, Thomsen disease, Neuromyotonia, Paramyotonia congenita, Centronuclear myopathy, Nemaline myopathy, Mitochondrial myopathy) - Myopathy - Periodic paralysis (Hypokalemic, Hyperkalemic) - Lambert-Eaton myasthenic syndrome