Chapter 58 Fetal Face and Neck Flashcards

1
Q

Congenital anomalies of the face affect 1 in ____ births.

A

600

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2
Q

The nasal pits are formed as the surface ______ thickens into the nasal _____ on each side of the frontal nasal prominence; as these plaecodes invaginate, the nasal pits are formed.

A

ectoderm, placodes

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3
Q

Off-axis, or nonmidline, encephaloceles have also been reported with _________.

A

amniotic band syndrome

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4
Q

premature closure of any or all six of the cranial sutures

A

craniosynostosis

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5
Q

Unusually misshapen skull with a clover-leaf appearance in the anterior view

A

Kleeblattschadal

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6
Q

Clover leaf skull has been associated with numerous skeletal dysplasias (most notably, _________) and ________

A

thanatophoric dysplasia , ventricomegaly

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7
Q

Premature closure of the metopic suture may cause the forehead to have an elongated tall appearance in the sagittal plane and appear triangular shaped in the axial plane.

A

trigonocephaly

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8
Q

obsurved in a fetus with a lemon-shaped skull (from spina bifida) or with skeletal dysplasias.

A

frontal bossing

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9
Q

with depressed or absent nasal bridge, is underdevelopment of the middle structures of the face.

A

Midface hypoplasia or maxillary hypoplasisa

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10
Q

median cleft face syndrome consisting of a range of midline facial defects involving the eyes, forehead, and nose.

A

Frontal dysplasia

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11
Q

Frontal dysplasia abnormalities include…

A

ocular hypertelorism, a variable bifid nose, a broad nasal bridge, a midline defect of the frontal bone, and extension of the frontal hairline to form a widow’s peak.

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12
Q

The optimal gest age for measurements of fetal NT is _____ weeks of gest.

A

11weeks-13 weeks 6 days

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13
Q

Fetal crown-rump should be within the range of ______ mm

A

45-84

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14
Q

A NT measurement greater than ____ mm is abnormal

A

3

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15
Q

enlarged tongue

A

macroglassia

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16
Q

Congenital overgrowth of tissues

A

Beckwith-Wiedemann Syndrome

17
Q

Beckwith-Wiedemann syndrome commonly co-exists with …

A

omphalocele, macroglossia and vescoromegaly, and organomegaly

18
Q

small chin

A

micrognathia

19
Q

Micrognathia is associated with many conditions that can be subdivided into three groups of anomalies:

A
  • Chromosome anomalies (trisomy 18 and triploidy)
  • skeletal dysplasias
  • Primary mandibular disorders (Pierre Robin syndrome and Trecher Collins syndrome)
20
Q

Ear malformation may be observed in _________

A

Goldenbar’s syndrome

21
Q

absent eyes

A

anophalmia

22
Q

small ears

A

Robert’s syndrome

23
Q

inadequate development of the ear

A

Treacher Collins Syndrome

24
Q

Periorbital masses…..

A

lacimal duct cysts (dacryocystoceles), dermoids, and hemangiomas.

25
Q

abnormal protrusion of the eye

A

exophthalmia

26
Q

Hypotelerism is associated with several syndromes and other anomalies, including ________, microcephaly, craniosynostoses, and __________.

A

holoprosencephaly, phenylketonuria (PKU)

27
Q

_________ is found im fetuses exposed to phenytomin (Dilantin)

A

hypertelorism

28
Q

Evaluation of the nasal triad should assess…

A
  • nostril symmetry -nasal septum integrity, and -continuity of the upper lip, to exclude cleft lip and palate.
29
Q

1 per ____ births in Native Americans are affected by cleft palate.

A

250

30
Q

Cleft palate occurs when the _________ fail to fuse at the midline.

A

lateral palatine processes

31
Q

Teratoma located in the oropharynx. These masses may be highly complex and contain solid, cystic, or calcified components.

A

epignathus

32
Q

Results from the malformation of the lymphatic system that leads to single or multilocuated lymph-filled cavities around the neck.

A

cystic hygroma

33
Q

The differential considerations for cystic hygromas include….

A

meningomyelocele, encephalocele, nuchal edema, brachial cleft cyst, cystic teratoma, hernagioma, and thyoglossal duct cyst.

34
Q

Neck teratomas are usually _______ and located _______. May have complex sonographic patterns

A

unilateral, anteriorly