Amyotrophic Lateral Sclerosis (ALS)
ALS is a progressive neurodegenerative disease of brain and
spinalcord resulting in death of nerves that controls voluntry
muscle movements. The disease causes weakness, atrophy, muscle
spasm throughout the body due to upper and lower motor neuron
degeneration.
Criteria for diagnosis
of ALS
- Signs of lower motor neuron (LMN) degeneration by clinical
electrophysiological or neuropathological examination
- Signs of upper motor neuron (UMN) degeneration by clinical
examinations
- Progressive spread of signs within a region or to other
regions, along with the abscences of
- Electrophysiological evidences of other diseases that might
explain the signs of LMN and UMN degenerations
- Neuroimaging evidences of other disease process that might
explain the clinical and electrophysiological signs
Diagnosis
- History and
physical examinations: the causes of ALS is head
injury, affected first degree relatives, but most of the cases thre
is no strong causative factor. In the neurological examination if
there is evidence of both upper and lower neuron symptoms it is
suggestive of ALS. Progression of the signs and
symptoms is the cradinal feature of ALS.The
symptoms progress insidiously without any remissions and relapses.
Signs of LMN is weakness, wasting and fasiculations in one or more
regions ( bulbar, cervical, thoracic,lumbosacral regions). Signs of
UND include increases tendon reflexes, pseudobalbar features,
Hoffmans reflex and extensor plantar reflexes). Assess the progess
of symptoms periodically.
- Electromyography:
to detect the electrical activity of the muscles. If the patient
has poor electrical activity without the presence of other diseases
suggestive of ALS
- Nerve
Conduction Velocity: It is helpful to rule out
peripheral neuropathy and myopathy
- Magnetic
resonance Imaging of Brain and s[pinal cord (MRI):
in initial stage of ALS the MRI is normal but it is helpfull to
rule out tumours and other neurological diseases
- Clinical
laboratary examinations to rule out viral
infections, other diseases.
Conclusion:
there is no specific confirmatory examination sfor ALS. Diagnostic
tests are performed to rule out other neurodegenarative diseases.
In ALS the only way to diagnosis is periodic examination to findout
the progress of the disease, because in ALS it is progressive in
nature but in other disorders most of the cases there is relapses
and relieves of symptoms.