AccessMedicine's Case of the Week: Amyotrophic Lateral Sclerosis

From: Pathophysiology of Disease Cases: Nervous System Disorders > Amyotrophic Lateral Sclerosis (Motor Neuron Disease)

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May 19, 2019
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Case:

A 43-year-old right-handed man presents to the clinic with gradual onset of right hand and arm weakness. He had been in good health and an avid golfer until a few weeks ago when he noted that he was having trouble keeping his club steady during his swing. His driving distance had markedly decreased, and he had begun to drop things that he was holding with his right hand. He had no numbness or other sensory symptoms. On physical examination, he appears well and has normal vital signs. He has mild wasting and fasciculations along his right brachioradialis muscle. His grip strength is 4 out of 5 on the right and 5 out of 5 on the left. He has absent reflexes in his right arm and 1+ reflexes on the left. An electromyelogram shows features of denervation, including increased numbers of spontaneous discharges in resting muscle, and a reduction in the number of motor units detected during voluntary contraction. A diagnosis of amyotrophic lateral sclerosis (ALS) is entertained.

Questions:

1: What are the presenting clinical symptoms and progression of the clinical course in ALS?

2: Which cells are affected in ALS?

3: What are some possible molecular mechanisms responsible for the pathologic changes?


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Julie Grishaw, ACNP

Senior Editor, McGraw-Hill Education

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