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Upper motor neuron lesion

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This articleneeds morereliable medical references forverification or relies too heavily onprimary sources. Please review the contents of the article andadd the appropriate references if you can. Unsourced or poorly sourced material may be challenged andremoved.Find sources: "Upper motor neuron lesion" – news ·newspapers ·books ·scholar ·JSTOR(August 2019)
Medical condition
Upper motor neuron lesion
The motor tract.
SpecialtyNeurology

Anupper motor neuron lesion (also known aspyramidal insufficiency) Is an injury or abnormality that occurs in the neural pathway above theanterior horn cell of the spinal cord ormotor nuclei of thecranial nerves. Conversely, alower motor neuron lesion affects nerve fibers traveling from the anterior horn of thespinal cord or the cranial motor nuclei to the relevant muscle(s).[1]

Upper motor neuron lesions occur in the brain or the spinal cord as the result ofstroke,multiple sclerosis,traumatic brain injury,cerebral palsy,atypical parkinsonisms,multiple system atrophy, andamyotrophic lateral sclerosis.

Symptoms

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Changes in muscle performance can be broadly described as theupper motor neuron syndrome. These changes vary depending on the site and the extent of the lesion, and may include:

  • Muscle weakness.[2] known as 'pyramidal weakness'
  • Sloth sign. Decreased control of active movement, particularly slowness
  • Spasticity, a velocity-dependent change in muscle tone
  • Clasp-knife response where initial higher resistance to movement is followed by a lesser resistance
  • Babinski sign is present, where thebig toe is raised (extended) rather than curled downwards (flexed) upon appropriate stimulation of the sole of the foot. The presence of the Babinski sign is an abnormal response in adulthood. Normally, during the plantar reflex, it causes plantar flexion and the adduction of the toes. In Babinski's sign, there is dorsiflexion of the big toe and abduction of the other toes. Physiologically, it is normally present in infants from birth to 12 months. The presence of the Babinski sign after 12 months is the sign of a non-specific upper motor neuron lesion.
  • Increaseddeep tendon reflex (DTR)
  • Pronator drift[3]

Corticospinal/pyramidal tract

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These are the neural tracts which descend in theventral horn of the spinal cord, carrying signals for voluntary movement of skeletal muscle. From their origin in theprimary motor cortex, these nerves pass via thecorona radiata to gather in theinternal capsule before crossing over to the opposite side (decussation) in themedullary pyramids and proceeding down the spinal cord to meetlower motor neurons in theanterior grey column.

Diagnosis

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During an exam, your doctor will look for signs of a nervous system problem by checking your:

  • Balance and coordination
  • Movement
  • Hearing, speech, and vision
  • Memory and concentration

Tests for diagnosis

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Treatment

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The treatment of an upper motor neuron lesion will be dependent on the underlying cause.

See also

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References

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  1. ^James D. Fix (1 October 2007).Neuroanatomy. Lippincott Williams & Wilkins. pp. 120–.ISBN 978-0-7817-7245-7. Retrieved17 November 2010.
  2. ^"upper motor neurone signs".GPnotebook.
  3. ^"The Precise Neurological Exam". Archived fromthe original on 2009-04-29. Retrieved2009-11-28.

External links

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Classification
Signs and symptoms relating to movement andgait
Gait
Coordination
Abnormal movement
Posturing
Paralysis
Weakness
Range of motion
Other
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