Biomedical Engineering Reference
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Frontalis muscle
Temporal
branch
Obicularis oculi
muscle
Nasalis muscle
Zygomatic
branch
Levator labii
superioris muscle
Zygomaticus minor
and major muscle
Buccal
branch
Orbicularis oris
muscle
Mentalis muscle
Depressor anguli
oris muscle
Cervical
branch
Mandibular
branch
FIGURE 5.15
The facial nerve and its major branches are depicted innervating some
of the major face muscles. (Reprinted with permission from Preston, D.
and Shapiro, B., Electromyography and Neuromuscular Disorders: Clinical-
Electrophysiologic Correlations , Elsevier, Philadelphia, PA, 2005.)
to scarring of the nerves in the lateral spinal column due to nerve death.
ALS unfortunately possesses a uniformly poor prognosis, being fatal in all
cases, with death on average of 3 years after onset with approximately 10% of
patients surviving longer. The diseases usually affect those above 55 years of
age but is sometimes also found in younger children. Several ALS variants have
been identified including progressive bulbar palsy, progressive muscular atro-
phy, and primary lateral sclerosis. Both upper and lower motor neurons are
affected whereas the sensory and autonomic functions are spared. Symptoms
include muscle atrophy, cramps, spreading weakness, slowness in movements,
and spasticity. Death usually results from respiratory failure as the nerves
controlling the respiratory process die and respiratory control is lost whereas
other complications include pulmonary embolus, sepsis, and pneumonia. At
this point in time, the exact etiology for ALS is still unknown but several
unproven speculations ranging from genetics, viral infections to toxic poison-
ing have been suggested.
Another group of MNDs, less common and less fatal is the atypical MNDs.
These diseases have similar symptoms to ALS but can be differentiated using
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