LMNL Lower Motor Neuro Lesion Flashcards
What is it
A lesion affecting the lower motor neurons (LMNs), which originate in the spinal cord or brainstem and directly innervate muscles. Leads to flaccid weakness, muscle atrophy, and loss of reflexes.
Clinical Features
✅ Key Signs of LMN Lesion:
Muscle weakness (paresis or paralysis) WITH atrophy 💪❌
Flaccidity (decreased muscle tone, hypotonia) 🛌
Hyporeflexia (reduced or absent deep tendon reflexes) 🦵❌
Fasciculations (involuntary muscle twitches) 🌀
Normal or absent Babinski sign (toes curl downward)
🚫 NO spasticity, hyperreflexia, or clonus (UMN signs).
Epidemiology
Common in nerve injuries, peripheral neuropathies, spinal cord diseases, and motor neuron diseases.
Can occur at any age depending on cause.
Age Groups Affected
• Infants & children: Spinal muscular atrophy (SMA), polio
• Young adults: Peripheral nerve injuries (trauma, Guillain-Barré Syndrome)
• Middle-aged to older adults: ALS, diabetic neuropathy, radiculopathies
Risk Factors
✅ Modifiable:
Diabetes (diabetic neuropathy) 🩸
Vitamin B12 deficiency (affects myelin, leading to neuropathy)
Toxins (alcohol, heavy metals, chemotherapy drugs)
Infections (poliovirus, syphilis, Lyme disease)
Compression (herniated discs, spinal stenosis)
🚫 Non-Modifiable:
Genetic disorders (SMA, ALS, Charcot-Marie-Tooth disease)
Aging-related nerve degeneration
Autoimmune conditions (Guillain-Barré Syndrome, myasthenia gravis)
Clinical Presentation
🔹 If Peripheral Nerve Lesion (e.g., Guillain-Barré, nerve trauma):
Flaccid paralysis/weakness in affected limb
Absent reflexes
Sensory loss may be present
Fasciculations in chronic cases
🔹 If Spinal Cord LMN Lesion (e.g., Polio, ALS, radiculopathy):
Weakness & atrophy in specific myotomes
Loss of reflexes at affected level
No upper limb involvement if lower cord affected
🔹 If Motor Neuron Disease (e.g., ALS – both UMN & LMN signs):
Muscle weakness with atrophy
Fasciculations
Normal cognition (no sensory loss)
Prognosis
🔹 Depends on the cause:
Guillain-Barré Syndrome: Can recover with treatment but may have residual weakness
Peripheral nerve injuries: May recover if axon regenerates (slow process)
ALS (both UMN & LMN affected): Progressive & fatal
Diabetic neuropathy: Can be managed but not reversed
Polio survivors: Can develop post-polio syndrome with worsening weakness later in life
🔹 Treatment & Management:
Physical therapy & rehabilitation 🏋️♂️
Vitamin supplementation (if nutritional cause) 💊
Immunotherapy for autoimmune causes (e.g., IVIG for GBS)
Surgical decompression for nerve compression syndromes
Tests
- Muscle strength & tone - checking for flaccidity & Atrophy
- Deep tendon reflexes - checking for HYPOreflexia
- Fasciculation test - involuntary muscle twitches
- Babinski sign (plantar reflex)