Muscle Weakness ; Lecture Flashcards

1
Q

Muscle weakness due to _________ disease is typically proximal, while weakness from _________ disease is distal.

A

muscle; nerve.

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2
Q

True/False: Bulbar involvement is characteristic of Myasthenia Gravis (MG).

A

True.

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3
Q

What are the key anatomical structures involved in motor function?

A

Motor cortex.
Medulla/spinal cord.
Anterior horn cell.
Motor neuron.
Neuromuscular junction (NMJ).
Muscle.

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4
Q

Myasthenia Gravis primarily affects the _________, while Duchenne Muscular Dystrophy involves the _________.

A

neuromuscular junction; muscle.

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5
Q

True/False: Stroke, multiple sclerosis (MS), and tumors can affect the motor cortex and spinal cord.

A

True.

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6
Q

What key aspects should be assessed in the history of a patient with muscle weakness?

A

Onset (sudden vs gradual).
Distribution (proximal vs distal, symmetrical vs asymmetrical).
Variability (fixed vs progressive).
Associated sensory features (e.g., tingling, numbness).

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7
Q

Symmetrical weakness suggests _________ causes, while asymmetrical weakness often indicates _________ or inflammatory causes.

A

genetic or metabolic; vasculitic.

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8
Q

Which toxins can cause peripheral neuropathy?

A

Alcohol, nitrous oxide, chemotherapy, amiodarone, and lead.

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9
Q

What are the most common causes of peripheral neuropathy?

A

Diabetes.
Alcohol.
Idiopathic causes (20%+).

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10
Q

Peripheral neuropathies can affect _________, _________, or both, and may involve _________, myelin, or both.

A

motor nerves; sensory nerves; axons.

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11
Q

What are the hallmark features of Myasthenia Gravis?

A

Fatigueable weakness.
Proximal limb involvement.
Ptosis and diplopia.
Bulbar symptoms (speech, swallowing).
Risk of respiratory failure.

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11
Q

True/False: Chronic peripheral neuropathies are usually length-dependent, starting in the legs.

A

True.

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12
Q

Myasthenia Gravis is associated with _________ dysfunction, including thymic hyperplasia and _________.

A

thymus; thymoma.

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13
Q

True/False: EMG with repetitive stimulation is more sensitive than antibody tests for diagnosing MG.

A

True.

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14
Q

How is MG treated?

A

Acetylcholine esterase inhibitors (e.g., pyridostigmine).
Immunosuppressants (steroids, azathioprine).
Thymectomy if thymoma is present.
Monitoring forced vital capacity (FVC).

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15
Q

_________ myopathy and _________ myopathy are common drug-induced muscle disorders.

A

Steroid; statin.

16
Q

True/False: Mitochondrial disorders may involve eye movement abnormalities and are associated with muscle disorders.

A

True.

17
Q

What tests are critical for evaluating neuropathy?

A

History and examination.
Nerve conduction studies (NCS).
EMG.
CSF study.
Neuropathy and vasculitic screens.

18
Q

A neuropathy screen includes _________, _________, and _________.

A

FBC; glucose; B12/folate levels.

19
Q

How is myopathy investigated?

A

Creatine kinase (CK).
EMG.
Muscle MRI.
Genetic testing.
Biopsy.

20
Q

A 50-year-old landlady reports tingling in her fingers and feet with clumsiness and frequent falls. What is the likely diagnosis?

A

Diabetic peripheral neuropathy.

21
Q

A 45-year-old reporter has numbness over the lateral two digits of the left hand. Phalen’s test is positive. What is the diagnosis?

A

Carpal tunnel syndrome

22
Q

In a myasthenic crisis, _________ and _________ functions should be closely monitored.

A

respiratory; bulbar.

23
Q

What are the key management strategies for neuromuscular diseases?

A

Multidisciplinary team (MDT) involvement.
Address breathing and swallowing issues.
Treat underlying causes.
Provide supportive care (e.g., physiotherapy, OT).

24
Q

_________ and _________ are critical red flags in neuromuscular emergencies.

A

Sudden respiratory distress; progressive bulbar dysfunction.

25
Q

True/False: Proximal muscle weakness typically involves difficulty with stairs, chairs, and hair grooming.

A

True

26
Q
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27
Q
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28
Q
A