Genetic Counseling Flashcards

1
Q

what happens in genetic counseling

A
  • communication to understand and adapt to the genetic component of health conditions
  • interpretation of family and medical hx to assess disease occurrence and recurrence
  • education about inheritance
  • counseling to promote informed choices and adaptation to the risk or condition
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2
Q

the leading cause of mortality and morbidity in the ph

A

breast ca

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3
Q

what is the nicca law

A

ra 11215: national integrated cancer control act of 2019

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4
Q

objectives of nicca law

A

read

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5
Q

red flags associated with hereditary ca: multiple cancers

A

a combination of cancers on the same side of the family

  • > 2 breast/ ovarian/ prostate/ pancreatic (hereditary breast and ovarian ca)
  • > 2 colorectal, endometrial, ovarian, gastric, pancreatic, other ca (lynch sydrome)
  • > 2 melanoma or pancreatic
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6
Q

red flags associated with hereditary ca: young ca

A

any 1 of the following at less/= 50 yo

  • breast
  • crc
  • endometrial
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7
Q

red flags associated with hereditary ca: rare ca

A

any 1 at any age

  • ovarian ca
  • breast: male or triple negative
  • crc with abnormal msi/ihc, msi associated histology
  • endometrial ca with abnormal msi-ihc
  • > /= 10 gi polyps adenomatous type
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8
Q

pre test counseling in the development of ca

A
  • 1: normal cells
  • 2: cell becomes mutated
  • 3: mutated cell rapidly divides
  • 4: growth of new blood vessels forming invasive tumor
  • 5: metastases
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9
Q

t/f mutation equates to having cancer

A

false, mutations INCREASE THE CHANCE OF HAVING CANCER

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10
Q

causes of cancer

A
  • hereditary 5-10% (present in every generation)
  • familial ca 10-25% (clustering that may or may not be due to a particular gene, can be environmental)
  • sporadic 60-75% (lifestyle, radiation, carcinogens)
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11
Q

most common pattern of inheritance for cancer

A

autosomal dominant

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12
Q

what is somatic testing

A
  • identified mutations in the tumor itself
  • performed on tumor tissue
  • patient has cancer
  • ordered by oncologist and patient does not consent
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13
Q

purpose of somatic testing

A

to identify treatment options or determine prognosis

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14
Q

what is germline testing

A
  • identifies mutations you were born with
  • samples taken from body
  • patient may be unaffected
  • ordered by genetic counselors and pts consent
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15
Q

purpose of germline testing

A
  • identify pts with inherited ca predisposition syndromes

- can be used to determine treatment in some cases

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16
Q

purpose of post test counseling

A
  • give information on what patients should do with the result
  • tell pt how the result can help him/her with management
  • needed when patients undergo hereditary testing
17
Q

possible results of genetic test

A
  • pathogenic variant detected or positive result
  • no pathogenic variant detected or negative result
  • variant of uncertain significance
18
Q

result when mutation is detected in the genes known to cause cancer

A

pathogenic variant detected or positive result

19
Q

result when no detected mutation in the genes known to cause cancer

A

no pathogenic variant detected or negative result

  • does not mean patient has no mutation
  • only cancer related mutations are tested
20
Q

result: mutation where more testing needs to be done

A

variant of uncertain significance

- lacks evidence if mutation can cause cancer

21
Q

main benefits of hereditary genetic testing

A
  • precision oncology: getting exact medication for mutation

- testing of at-risk family members

22
Q

t/f if vus is present in a patient that already has cancer, that patient has a poor prognosis

A

true