Chapter 25 (The Fetal Face and Neck) Flashcards

1
Q

The absence of the eyes is termed:

A

anophthalmia

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2
Q

A reduction in the distance between the orbits is referred to as:

A

hypotelorism

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3
Q

The most frequently encountered chromosomal abnormality associated with holoprosencephaly is:

A

Trisomy 13

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4
Q

The fetal lip typically closes by:

A

8 weeks

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5
Q

The most common cause of hypertelorism:

A

anterior cephalocele

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6
Q

Macroglossia is most commonly found with:

A

Beckwith-Wiedemann syndrome

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7
Q

An oral teratoma is referred to as:

A

epignathus

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8
Q

Cleft lip and cleft palate may exist with:

A

Amniotic band syndrome, holoprosencephaly, Trisomy 13

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9
Q

An increase distance between the orbits is referred to as:

A

hypertelorism

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10
Q

The optimal scan plane to visualize micrognathia is:

A

sagittal

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11
Q

A cystic hygroma is the result of:

A

an abnormal accumulation of lymphatic fluid within the soft tissue

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12
Q
A cystic hygroma is found in all of the following conditions except:
A. Edwards syndrome
B. Hydranencephaly
C. Turner sydrome
D. All of the above
A

Hydranencephaly

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13
Q

Nuchal thickening is most commonly associated with:

A

Down syndrome

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14
Q

Micrognathia is a condition found in:

A

Trisomy 18

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15
Q

The most common location of a cystic hygroma is within the:

A

neck

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16
Q

An unusual protuberance of the tongue is termed:

A

macroglossia

17
Q

Facial anomalies, when discovered, should prompt the sonographer to analyze the brain closely for signs of:

A

holoprosencephaly

18
Q

The measurement obtained between the lateral walls of the orbits is referred to as the:

A

binocular diameter

19
Q

A large, mostly cystic mass is noted in the cervical spine region of a fetus. This likely represents a :

A

cystic hygroma

20
Q

A group of abnormalities associated with the entrapment of fetal parts and fetal amputations is:

A

amniotic band syndrome

21
Q

The growth disorder syndrome synonymous with organ, skull, and tongue enlargement is:

A

Beckwith-Wiedemann syndrome

22
Q

Which of the following is also referred to as Patau Syndrome?

A

Trisomy 13

23
Q

Close-set eyes and a nose with a single nostril is termed:

A

cebocephaly

24
Q

An abnormal division in the lip is referred to as:

A

cleft lip

25
Q

Fusion of the orbits is termed:

A

cyclopia

26
Q

The thickness of the nuchal fold in the second trimester should not exceed:

A

6mm

27
Q

A small mandible is termed:

A

micrognathia

28
Q

The condition in which there is no nose and a proboscis separating two close-set orbits is:

A

ethmocephaly

29
Q
All of the following are sonographic features of holoprosencephaly except:
A. cystic hydroma
B. proboscis with cyclopia
C. Fused thalamus
D. Monoventricle
A

A. cystic hydroma