Chapter·OB/GYNScreening tests

Carrier screening for genetic disordersDownloads

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Sample Questions

1

A genetic counselor sees a family for the first time for genetic assessment. The 24-year-old businessman and his 19-year-old sister are concerned about having a mutant allele and have decided to get tested. Their grandfather and great aunt both have Huntington’s disease which became apparent when they turned 52. Their father who is 47 years old appears healthy. The geneticist discusses both the benefits and risks of getting tested and orders some tests. Which of the following tests would best provide evidence for whether the siblings are carriers or not?

AGel electrophoresis

BRestriction enzyme digestion products

CPolymerase chain reaction

DPyrosequencing

EDNA isolation and purification

2

A 19-year-old male from rural West Virginia presents to his family medicine doctor to discuss why he is having trouble getting his wife pregnant. On exam, he is 6 feet 2 inches with a frail frame and broad hips for a male his size. He is noted to have mild gynecomastia, no facial hair, and small, underdeveloped testes. He claims that although he has a lower libido than most of his friends, he does have unprotected sex with his wife. His past medical history is notable for developmental delay and difficulties in school. What is the most likely chromosomal abnormality in this patient?

ATrisomy 13

B45: XO

CTrisomy 21

D47: XYY

E47: XXY

3

A 35-year-old woman gravida 2, para 1, comes to the physician for her first prenatal visit. Pregnancy and delivery of her first child were uncomplicated. She is not sure about the date of her last menstrual period. Pelvic examination shows a uterus consistent in size with a 10-week gestation. An ultrasound examination confirms the gestational age and shows one fetus with no indication of multiple gestations. During counseling on pregnancy risks and possible screening and diagnostic tests, the patient states she would like to undergo screening for Down syndrome. She would prefer immediate and secure screening with a low risk to herself and the fetus. Which of the following is the most appropriate next step in management at this time?

ANuchal translucency, pregnancy-associated plasma protein-A, human chorionic gonadotropin

BMaternal serum α-fetoprotein, human chorionic gonadotropin, unconjugated estriol, and inhibin A

CChorionic villus sampling

DAmniocentesis

ECell-free fetal DNA testing

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