Clinical Manifestations
Pathophysiology
Diagnosis
Treatment
Miscellaneous
100

This disease includes Progressive weakness begins in either the limbs or bulbar muscles, eventually spreading throughout the body.

What is Progressive motor weakness

100

A nuclear protein becomes mislocalized to the cytoplasm in motor neurons, forming toxic aggregates and impairing RNA regulation.

TDP-43 proteinopathy

100

This electrodiagnostic study evaluates the electrical activity of muscles. In this condition, it often reveals active denervation and reinnervation in multiple regions, with normal sensory nerve function, supporting a motor neuron disorder.

Electromyography (EMG) showing widespread denervation and reinnervation

100

This glutamate pathway modulator modestly extends survival by reducing excitotoxicity in the CNS.

Riluzole

100

This enzyme mutation was the first genetic cause discovered and is still studied

Superoxide dismutase 1 (SOD1) mutation

200

This disease has early symptoms may include difficulty speaking, slurred speech, and trouble swallowing, often leading to weight loss.

Bulbar onset symptoms

200

A hexanucleotide repeat expansion in a specific gene results in the production of toxic RNA and abnormal proteins that contribute to motor neuron loss.

C9orf72 mutation

200

Diagnosis is primarily clinical but requires exclusion of other conditions through imaging, bloodwork, and neurophysiological testing.

Diagnosis of exclusion

200

Approved in 2017, this antioxidant slows functional decline and is often given intravenously in cycles.

Edaravone

200

This familial form of the condition follows an autosomal dominant inheritance pattern and may appear in multiple generations.

 autosomal dominant inheritance

300

This disease includes, muscle twitching and muscle cramps occur frequently, especially in the arms, legs, shoulders, and tongue.

Fasciculations and cramps

300

Degeneration of both upper and lower motor neurons leads to a combination of spasticity, hyperreflexia, muscle atrophy, and muscle twitching.

motor neuron degeneration

300

normal sensory nerve conduction studies help differentiate this condition from peripheral neuropathies.

Preserved sensory nerve conduction on NCS

300

Coordinated care involving neurology, physical therapy, respiratory therapy, and palliative services improves symptom management and survival, especially when assisted ventilation is used.

Multidisciplinary care with non-invasive ventilation

300

Most individuals with this condition eventually require assistive devices for mobility and respiratory support, due to lack of muscle strength

Progressive physical disability

400

As the disease progresses, breathing becomes more difficult due to weakening of the diaphragm and intercostal muscles.

Respiratory muscle weakness

400

Excess extracellular glutamate, due to impaired astrocytic uptake, leads to excitotoxicity and neuronal injury.

Glutamate excitotoxicity

400

This imaging technique may be used to rule out structural causes of upper motor neuron signs, such as cervical spondylotic myelopathy.

MRI of the brain and spinal cord

400

Management includes interventions tailored to specific symptoms, such as feeding tube placement for dysphagia, antispasmodic medications for muscle stiffness, and assistive communication devices for speech loss.

Supportive symptom management

400

About 10% of cases are inherited, often through an autosomal dominant mutation in genes like SOD1 or TARDBP.

Familial inheritance patterns

500

Despite widespread motor decline, sensation, bowel/bladder control, and eye movements typically remain intact.

Preserved sensory and autonomic function

500

The condition presents with progressive limb weakness, muscle twitches, and spasticity, often with preserved sensory and cognitive function.

Progressive motor neuron disease

500

This simplified diagnostic framework requires progressive motor impairment with clinical signs of both upper and lower motor neuron dysfunction, and was introduced in 2019 to allow earlier diagnosis of motor neuron disease.

Gold Coast Criteria

500

This approach emphasizes comfort, psychological support, and quality of life in advanced stages. It involves pain control, respiratory support, and end of life planning, often provided alongside standard medical care.

Palliative care

500

A well known physicist who made groundbreaking contributions to cosmology despite living with this condition for over 50 years

Stephen Hawking