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

Multifocal motor neuropathy


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


Entities / Miasms
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
    1. MMN affects predominantly (but not exclusively) the upper limbs
    2. MMN usually lacks bulbar or respiratory involvement
    3. MMN is associated with less atrophy, unless it becomes severe or longstanding
    4. 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
    5. MMN has no upper motor neuron signs
    6. 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.

  1. 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.