Cystic Fibrosis Flashcards

1
Q

In CF where is the mutation

A

chromosome 7

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2
Q

What is decreased in Cystic Fibrosis?

A

decrease in water and sodium in respiratory trac

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3
Q

What is a result of CF bacteria buildup?

A

Pneumonia

Respiratory Failure

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4
Q

What is the treatment for CF?

A

No cure, just to ease and reduce complications
Antiboitics to stop lung infections
antiinflam drugs for airways
administration of oral pancreatic enzymes

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5
Q

What happens in the lung with CF?

A

person is unable to expire, causing build up secretion - end up with thick mucus, mucus clogs the airways and traps bacteria

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6
Q

What are some digestive signs

A
thick mucus blocks tubes that carry digestive enzymes from your pancreas to your small intestine causing 
S  Smelly stool
 I  Intestinal blockage (meconium ileus)
P  Poor weight gain and growth
S   Severe constipation
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7
Q

Can the signs of CF be delayed

A

yes

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8
Q

What is a symptom of CF involving sweat

A

salty sweat

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9
Q

What are some respiratory signs

A

L lung infections
E exercise intolerance
T thick sticky mucus

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10
Q

What does the CFTR do

A

create channels on the cell surface to allow the movement of chloride (a component of salt) in and out of the cell.

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11
Q

What happens in CF relating to the CFTR

A

the CFTR is either malformed or missing causing an imbalance of chloride ions in and out of cells

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12
Q

who is most effected

A

caucasians, 1 in 2500 to 3500

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13
Q

What are some ways CF is diagnosed

A

newborn screening

genetic and sweat test

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14
Q

What is the most common cause of death from CF

A

Pneumonia

Respiratory Failure

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