
Chapter 55
Presentation
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Health Sciences
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University
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Practice Problem
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Medium
Megan Mullins
Used 2+ times
FREE Resource
59 Slides • 30 Questions
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Multiple Choice
Which of the following statements about congenital anomalies is correct?
Major congenital anomalies are found in 3 of every 100 births.
Minor birth defects complicate less than 5% of births.
Sonographers do not screen for unsuspected anomalies.
All congenital anomalies are detected before birth.
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Multiple Choice
Why is it important to identify congenital anomalies during the prenatal period?
to enable early intervention and informed decision-making.
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Multiple Choice
Which of the following must be determined prior to performing chorionic villus sampling?
Fetal life, morphology, and age
Mother's blood type only
Placental weight
Father's genetic history
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Fill in the Blanks
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Multiple Choice
When is chorionic villus sampling performed?
Week 11-13
Week 10-12
Week 10-14
Week 11-14
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Multiple Choice
Which of the following steps is NOT part of the chorionic villus sampling procedure?
US guides needle to placenta
Catheter inserted through the needle
Catheter "sucks" up placental tissue
Amniotic fluid is withdrawn
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Open Ended
Describe the difference between transabdominal and transcervical chorionic villus sampling as shown in the diagrams.
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Multiple Choice
Why is there a gestational age limit of 12 weeks for embryoscopy?
Because of the fusion of amnion and chorion
Because fetal lung maturity is reached
Because the placenta is fully developed
Because the fetus is too large after 12 weeks
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Multiple Select
Which of the following are uses of amniocentesis?
Relieve polyhydramnios
Predict Rh isoimmunization
Document fetal lung maturity
Direct viewing of the embryo
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Multiple Choice
For which group of patients is amniocentesis especially recommended?
Patients at risk for chromosomal or biochemical disorders
Patients with normal triple screen results
Patients with no history of congenital abnormalities
Patients with low maternal age
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Multiple Choice
Amniocentesis is ideally performed between what weeks gestation?
11 to 16 weeks gestation
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Multiple Choice
Which of the following is a key step in performing amniocentesis in multiple gestations?
indigo carmine dye is used to distinguish amniotic cavities
Only one fetus is evaluated for anatomy and growth
RhoGam is administered to all patients regardless of Rh status
Zygocity is not determined
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Multiple Select
Which of the following are risks associated with amniocentesis?
Miscarriage
Preterm labor
Subchorionic hemorrhage
Gestational diabetes
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Multiple Choice
What is the main difference in the ultrasound appearance when the needle is inserted parallel versus at an angle to the transducer during amniocentesis?
Only the tip is represented when parallel, but the whole needle may be seen at an angle
The parallel approach is more dangerous
The angled approach always shows the needle tip clearly
Both approaches are equally safe
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Multiple Choice
Cordocentesis is commonly used for?
administering fetal vitamins
performing routine ultrasound of umbilical cord
transfusions in isoimmunization
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Fill in the Blanks
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Multiple Select
AFP can be found in which of the following fetal structures?
Spine
GI tract
Kidneys
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Multiple Choice
How does AFP reach the amniotic fluid?
through maternal blood.
through fetal urination.
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Multiple Choice
At what weeks do AFP levels peak?
15 to 18 weeks
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Multiple Select
Which markers are evaluated in the quadruple screen for prenatal screening?
AFP
hCG
Unconjugated estriol
PAPP-A
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Fill in the Blanks
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Multiple Choice
What is Aneuploidy?
a type of genetic mutation that affects DNA sequence.
an abnormal number of chromosomes.
a process of cell division that results in identical chromosomes.
a condition where chromosomes are duplicated.
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Multiple Choice
What is mosaicism?
the process of creating a mosaic artwork.
the mixing of different species in an ecosystem.
abnormal interaction of one or more genes and environmental factors
the presence of a mutation in a portion of an individual's cell.
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Multiple Choice
How many pairs of autosomes are present in a normal human karyotype?
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Multiple Choice
What is shown in the karyotype that has 3 of chromosome 13?
Trisomy 13
Trisomy 18
Trisomy 21
Monosomy X
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Multiple Choice
What is another name for Trisomy 21?
Edward
Patau
Down
Turner
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Multiple Choice
Which chromosomal abnormality is characterized by holoprosencephaly, single umbilical artery, and micrognathia
Trisomy 21
Trisomy 18
Trisomy 13
Turner syndrome
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Multiple Choice
What chromosomal abnormality is characterized by a cystic hygroma, short femurs, and female gender?
Klinefelter syndrome
Down syndrome
Edwards Syndrome
Turner syndrome
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Multiple Choice
Which chromosomal abnormality is characterized by rocker bottom feet, strawberry shaped cranium, and overlapping fingers?
Trisomy 18
Trisomy 21
Trisomy 13
Turner
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Multiple Choice
Which chromosomal abnormality is characterized by echogenic cardiac focus, ventriculomegaly, duodenal atresia, and an absent nasal bone?
Trisomy 18
Trisomy 21
Trisomy 13
Turner
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