Myasthenia Gravis Flashcards

1
Q

where does MG act?

A

at the NMJ

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2
Q

MG is characterized by…

A

FLUCTUATING weakness and fatigability of skeletal muscles

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3
Q

what is the hallmark of MG

A

muscle weakness that increases during activity and improves with rest

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4
Q

What is the pathogenesis of MG

A

autoantibodies impact the NMJ POSTsynaptic ACh receptors

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5
Q

what is lamber-eaton myasthenic syndrome

A

a related pathology to MG but it is caused by autoantibodies to the PREsynaptic ACh receptor membrane

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6
Q

what is the etiology of MG

A

atuoimmune disorder assoc with thymus disorders

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7
Q

How does MG impact ACh receptors

A

anti-ACh-receptor antibodies are produced by the body which leads to a decrease in available ACh receptors for transmitting ACh across the NMJ

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8
Q

how is MG diagnosed

A

ACh-esterase inhibitors will improve patient symptoms OR EMG testing OR immunologic testing for anti-ACh-receptor Abs in the blood

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9
Q

MG clinical presentation

A

fluctuating weakness of proximal muscles!!!

muscles of the eyes and CN muscle often first to show signs!!!

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10
Q

describe the course of MG

A

variable, but slowly progressive. exacerbations may drive an MG crisis that endangers respiratory status

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11
Q

treatment options for MG other than PT

A

thymectomy (to stop autoantibody production), AChE inhibitors, corticosteroids for immune suppression, plasmapheresis, IVIG

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12
Q

As a PT, what can we offer MG patients

A

energy conservation and pacing, respiratory training, balance training, strengthening and aerobic training after exacerbation

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