Motor neuropathy: Difference between revisions
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=== Clinic === | |||
* '''MMN''' is a almost a pure progressive [[motor neuropathy]] of extremities. | |||
* Etiology: Autoimmune | |||
* It is sometimes mistaken for [[ALS, Amyotrophic Lateral Sclerosis remedies|ALS]] because of the similarity in the clinical picture, especially if muscle fasciculations are present | |||
=== MMN vs ALS === | |||
* Unlike ALS, which affects both [[Upper motor neuron, UMN|upper]] and [[LMN, Lower Motor Neuron|lower motor neuron]] pathways, MMN involves only LMN pathway, specifically peripheral nerves emanating from the lower motor neurons. | |||
* MMN can be difficult to distinguish from [[Motor Neuron Disease|motor neuron disease]] since both present with Asymmetric, Progressive, Distal weakness without Numbness. Here is some distinguishing points | |||
*# MMN affects predominantly (but not exclusively) the upper limbs | |||
*# MMN usually lacks bulbar or respiratory involvement | |||
*# MMN is associated with less atrophy, unless it becomes severe or longstanding | |||
*# Cramps and fasciculations can occur in motor neuron disease but are less prominent than in MMN, occurring in up to 50% of patients with MMN | |||
*# MMN has no upper motor neuron signs | |||
*# The most important distinguishing feature of MMN is conduction block which is pathognomonic electrophysiological pattern of MMN. <ref>Lawson VH, Arnold WD. Multifocal motor neuropathy: a review of pathogenesis, diagnosis, and treatment. Neuropsychiatr Dis Treat. 2014 Apr 5;10:567-76. doi: 10.2147/NDT.S39592. PMID: 24741315; PMCID: PMC3983019.</ref><br /> | |||
=== Sign / Symptoms === | |||
* Usually beginning in one or both hands | |||
* Weakness / Muscle atrophy | |||
* Cramping: It usually involves very little pain, however, muscle Cramps/ Spasms / Twitches can cause pain. | |||
* Profuse [[Fasciculation|fasciculations]] (Twitching). | |||
* The symptoms are progressive over long periods, often in a stepwise fashion | |||
* Sensory nerves are usually unaffected | |||
* Wrist / Foot drop a are common symptoms | |||
* Gradual loss of finger extension | |||
* Cold & hot temperatures exacerbate MMN symptoms to such an extent, unlike other neuropathies, that this temperature response is being investigated as a diagnostic tool. | |||
* MMN is not fatal, however lead to significant disability | |||
=== Entities / Miasms === | |||
{| class="wikitable" | |||
! | |||
!PLV | |||
!TBE | |||
!CJD | |||
!JE | |||
|- | |||
|[[Motor neuropathy]] | |||
| +++ | |||
| +++ | |||
| +++ | |||
| +++ | |||
|- | |||
|[[Spasm]] | |||
| +++ | |||
| | |||
| +++ | |||
| | |||
|} | |||
Spasm as a dependent entity, maybe present. | |||
* [[PLV, Polio Virus|PLV]] | * [[PLV, Polio Virus|PLV]] |
Revision as of 21:39, 20 May 2023
Clinic
- Motor Neuropathy is an entity which occurs if the motor nerves which control muscle movements become damaged.
- As with sensory neuropathy, the parts of the body most likely to be affected are the feet, hands, legs and arms.
- It arises from disease processes affecting the motor axon and/or its surrounding myelin, however Lower motor neuron syndrome (LMNS) arises from a disease process affecting the spinal motor neuron itself.
Related disease
Sign / Symptoms
- Fasciculation / Twitching: Note that fasciculations or Twitching would be the used as an eliminated rubric
- Impaired balance and coordination
- Muscle weakness
- Muscle atrophy
Asymmetric Paralysis
Hemiparesis |
|||
Clinic
- MMN is a almost a pure progressive motor neuropathy of extremities.
- Etiology: Autoimmune
- It is sometimes mistaken for ALS because of the similarity in the clinical picture, especially if muscle fasciculations are present
MMN vs ALS
- Unlike ALS, which affects both upper and lower motor neuron pathways, MMN involves only LMN pathway, specifically peripheral nerves emanating from the lower motor neurons.
- MMN can be difficult to distinguish from motor neuron disease since both present with Asymmetric, Progressive, Distal weakness without Numbness. Here is some distinguishing points
- MMN affects predominantly (but not exclusively) the upper limbs
- MMN usually lacks bulbar or respiratory involvement
- MMN is associated with less atrophy, unless it becomes severe or longstanding
- Cramps and fasciculations can occur in motor neuron disease but are less prominent than in MMN, occurring in up to 50% of patients with MMN
- MMN has no upper motor neuron signs
- The most important distinguishing feature of MMN is conduction block which is pathognomonic electrophysiological pattern of MMN. [1]
Sign / Symptoms
- Usually beginning in one or both hands
- Weakness / Muscle atrophy
- Cramping: It usually involves very little pain, however, muscle Cramps/ Spasms / Twitches can cause pain.
- Profuse fasciculations (Twitching).
- The symptoms are progressive over long periods, often in a stepwise fashion
- Sensory nerves are usually unaffected
- Wrist / Foot drop a are common symptoms
- Gradual loss of finger extension
- Cold & hot temperatures exacerbate MMN symptoms to such an extent, unlike other neuropathies, that this temperature response is being investigated as a diagnostic tool.
- MMN is not fatal, however lead to significant disability
Entities / Miasms
PLV | TBE | CJD | JE | |
---|---|---|---|---|
Motor neuropathy | +++ | +++ | +++ | +++ |
Spasm | +++ | +++ |
Spasm as a dependent entity, maybe present.
- ↑ Lawson VH, Arnold WD. Multifocal motor neuropathy: a review of pathogenesis, diagnosis, and treatment. Neuropsychiatr Dis Treat. 2014 Apr 5;10:567-76. doi: 10.2147/NDT.S39592. PMID: 24741315; PMCID: PMC3983019.