Lower motor lesion Flashcards
What is a lower motor neuron (LMN) lesion?
A lesion affecting the motor neurons that directly innervate skeletal muscles, typically located in the anterior horn of the spinal cord, brainstem, or peripheral nerves.
What are fasciculations, and how are they related to LMN lesions?
Fasciculations are involuntary muscle twitches, often seen in LMN lesions as a sign of ongoing denervation.
What happens to deep tendon reflexes in LMN lesions?
Hyporeflexia or areflexia (absent or diminished reflexes) is common.
What type of weakness is associated with LMN lesions?
Flaccid weakness with reduced muscle tone (hypotonia).
How does muscle atrophy appear in LMN lesions?
Muscle atrophy is pronounced due to lack of neural input to the muscles.
What is the typical muscle tone in LMN lesions?
Muscle tone is typically reduced or flaccid.
What does a normal Babinski sign indicate in an LMN lesion?
A normal Babinski sign (flexion of the toes) is typically present in LMN lesions.
What types of reflex changes are seen in LMN lesions?
Decreased or absent reflexes, also known as hyporeflexia or areflexia.
How is the gait affected in LMN lesions?
Gait can be weak or waddling, depending on which muscles are affected.
What type of motor unit activity is seen in electromyography (EMG) for LMN lesions?
Denervation potentials, such as fibrillations and positive sharp waves.
How does an LMN lesion affect the distribution of weakness?
Weakness is typically focal and follows the distribution of affected nerves or spinal segments.
How can sensory changes help differentiate between LMN and UMN lesions?
LMN lesions often accompany sensory loss if the peripheral nerve is affected, whereas UMN lesions typically do not.
What causes flaccid paralysis in LMN lesions?
Loss of input from motor neurons to the muscles results in flaccid paralysis.
How is muscle tone different in LMN lesions compared to UMN lesions?
LMN lesions result in hypotonia or flaccidity, while UMN lesions cause spasticity.
What is the difference between primary and secondary atrophy in LMN lesions?
Primary atrophy is due to direct denervation of muscles, while secondary atrophy occurs due to disuse.
What part of the motor system is affected by LMN lesions?
The anterior horn cells, cranial nerve motor nuclei, and peripheral nerves.
How do LMN lesions affect speech if cranial nerves are involved?
Dysarthria (slurred speech) can occur if cranial nerves, such as the hypoglossal nerve, are affected.
What is the typical progression of muscle atrophy in LMN lesions?
Atrophy usually progresses over time, especially in long-standing LMN lesions.
What cranial nerve palsies are commonly seen with LMN lesions?
LMN lesions can involve facial nerve palsy, hypoglossal nerve palsy, or oculomotor nerve palsy.
What can cause LMN lesions in the peripheral nerves?
Peripheral neuropathies, trauma, or compression (e.g., carpal tunnel syndrome).
How does the presence of fasciculations help diagnose LMN lesions?
Fasciculations are characteristic of LMN lesions due to motor unit instability.
What is the most common cause of LMN lesions affecting the anterior horn cells?
Amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA) are common causes.
How can Guillain-Barré syndrome present as an LMN lesion?
It causes ascending paralysis with LMN signs like hyporeflexia and flaccidity.
What is the difference between radiculopathy and peripheral neuropathy in LMN lesions?
Radiculopathy affects nerve roots, while peripheral neuropathy affects distal nerves.
What is the role of nerve conduction studies (NCS) in diagnosing LMN lesions?
NCS can show slowed conduction velocities or decreased amplitude, indicating peripheral nerve damage.
What reflex finding would you expect in a patient with an LMN lesion in the sciatic nerve?
Absent ankle reflex and weakness in leg muscles innervated by the sciatic nerve.
How do LMN lesions of the facial nerve typically present?
Bell’s palsy, which causes unilateral facial weakness affecting both upper and lower facial muscles.
What is the hallmark of an LMN lesion in spinal muscular atrophy (SMA)?
Progressive muscle wasting and weakness, especially in the limbs.