Pathology II Flashcards

1
Q

What is the genetic cause of Duchenne Muscular Dystrophy?

A

X-linked recessive trait

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2
Q

Are some of the first symptoms distal or proximal muscle weakness in Duchenne Muscular Dystrophy?

A

Proximal muscle weakness

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3
Q

What is used to examine electrical activity in muscles?

A

electromyography(EMG)

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4
Q

What is the classic presentation for Erb’s Palsy?

A

loss of shoulder function, loss of elbow function, loss of forearm supination, and hand positioned in pinch grip

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5
Q

What cervical roots are affected by Erb’s Palsy?

A

C5 and C6

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6
Q

What measures the electrical activity of the brain and is the most common test used to confirm the diagnosis of epilepsy?

A

Electroencephalogram

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7
Q

You should call 911 if a seizure last longer than…?

A

5 minutes

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8
Q

After a seizure is over what position should you place someone in to allow them to recover?

A

left side to avoid choking in case they vomit (food stays due to C shaped curve in stomach)

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9
Q

What is another name for Guillain-Barre Syndrome?

A

Acute Polyneuropathy

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10
Q

What are the initial symptoms of GBS?

A

distal symmetrical motor weakness and mild distal sensory impairments and transient paresthesias (burning tingling sensation)

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11
Q

During the acute stage of GBS what should a PT do?

A

limit overexertion and fatigue to avoid exacerbation of symptoms

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12
Q

With huntington’s disease why do ventricles of the brain become enlarged?

A

secondary to atrophy of basal ganlgia

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13
Q

With huntington’s disease there is often a decrease in activity and quantity of what 2 neurons?

A

gamma-aminobutryric acid (GABA) neurons
and
Acetylcholine neurons

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14
Q

What is choreathetosis?

A

the occurrence of involuntary movements in a combination of chorea (irregular migrating contractions) and athetosis (twisting and writhing).

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15
Q

Patient education with Huntington’s disease should focus on?

A

prone lying, stretching, prevention of deformity and contracture, and safety with mobility

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16
Q

Initial symptoms for this disease include paresthesias, sensory changes, clumsiness, weakness, ataxia, balance dysfunction, and fatigue?

A

Multiple Sclerosis

17
Q

85% of patients with MS are classified as having what type of MS?

A

relapsing-remitting

18
Q

What immunomodulatory medications are prescribed for multiple sclerosis?

A

ABC drugs

19
Q

What time of day should MS patients perform a submaximal exercise program?

A

in the morning when the patient is rested

20
Q

What autoimmune disease process is typically associated with an enlarged thymus?

A

Myasthenia Gravis

21
Q

What are the 2 cardinal signs of Myasthenia Gravis?

A
  1. extreme fatiguability

2. skeletal muscle weakness that can fluctuate within minutes or over an extended period of time

22
Q

What muscles are typically affected first and how does it present with Myasthenia Gravis?

A

Ocular Muscles –> presents as ptosis and diplopia

23
Q

In addition to taking drugs to inhibit actelcholinesterase for patients with Myasthenia Gravis what other drugs may be used to diminish symptoms of weakness and fatigue?

A

Coritcosteroids

24
Q

Physical therapy for Myastehnia Gravis should include energy conservation techniques and should be careful to avoid what?

A

overexertion

25
Q

Are proximal or distal muscles for affected typically with Myasthenia Gravis?

A

proximal

26
Q

What are three signs of a myasthenia “crisis”?

A

Respiratory difficulty, swallowing issues, labored talking/chewing

27
Q

What condition is characterized by damage or disease that affect multiple peripheral nerves including motor, sensory, and autonomic nerves?

A

Polyneuropathy

28
Q

What condition is characterized my increased demands placed on reinnervated denervated muscles via collateral spouting leading to deterioration of these nerves over time?

A

Post-Polio Syndrome

29
Q

How often and what type of exercise should be performed with post-polio syndrome?

A

AVOID intense exercise leading to fatigue or exhaustion and perform exercise every other day to allow for recovery

30
Q

what conditions causitive factor includes deletion of chromosome 15?

A

Prader-Willi Syndrome

31
Q

What condition is characterized by physical attributes of small hands, feet, sex oragans and almond sahpe eyes as well as behavioral attributes of constant desire for food?

A

Prader-Willi Syndrome

32
Q

In addition to to down syndrome what is another pediatric condition characterized by hypotonia?

A

Prader-Willi Syndrome