brain, skeleton, NTD, lung specific Flashcards

(72 cards)

1
Q

brachycephaly association

A

trisomy 21

round, short head

BPD increases GA

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2
Q

dolichocephaly BPD __ GA

A

decreases

long, narrow head

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3
Q

strawberry sign head association

A

trisomy 18

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4
Q

lemon sign head association

A

spina bifida

bilat concavity of front head

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5
Q

cloverleaf skull association

A

isolated OR skeletal dysplasia

aka craniosynostosis

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6
Q

spalding sign head association

A

fetal demise

flattened, misshapen head with overlapping sutures

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7
Q

neural tube fuses by __ GA

A

6w

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8
Q

encephaly aka

A

cranial NTDs

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9
Q

absence of calvarium (skull) with presence of varying amounts of brain tissue

A

exencephaly

severe open NTD

++ MSAFP, acetylcholinesterase

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10
Q

absence of calvarium (skull) and forebrain

A

anencephaly

severe open NTD

++ MSAFP, acetylcholinesterase

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11
Q

anencephaly = failure of neural tube to close at __ end

A

cephalic

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12
Q

anencephaly associations

A

myeloschisis/ rachiscisis

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13
Q

anencephaly vs. acephaly

A

acephaly is absence of whole head

anencephaly is absence of forebrain and skull

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14
Q

brain tissue through fissure in occiput so brain and spinal cord occupy a single cavity

A

iniencephaly

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15
Q

iniencephaly = defect in occipital bone with enlarged ++

A

foramen magnum

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16
Q

which encephaly will demonstrate cervical hyperextension and difficulty locating T and C spinal components

A

iniencephaly

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17
Q

herniation of brain tissue via defect in skull; can be symmetrical or asymmetrical, open or closed

A

encephalocele

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18
Q

cause for asymmetric encephalocele

A

amniotic band syndrome

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19
Q

encephalocele with polydactyly and a form of renal cystic dysplasia

A

meckel-gruber syndrome

ddx trisomy 13

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20
Q

what is the communication between the 3rd and 4th ventricles of the fetal brain

A

cerebral aqueduct

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21
Q

CPC usually normal and regress, but associated with trisomy __

A

18

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22
Q

general term for enlargement of cerebral ventricles

A

ventriculomegaly

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23
Q

normal lat vent measurement

A

<10mm

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24
Q

enlarged ventricle allowing choroid plexus to move toward gravity dependent portion of the brain

A

dangling choroid sign

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25
what is the normal angle of the choroid plexus
20-25 ^
26
dangling choroid sign associated with __
hydrocephalus due to obstruciton
27
ventricular dilatation due to obstruction between site of CSF production and absorption
hydrocephalus
28
one of the most common causes for hydrocephalus
aqueductal stenosis
29
sono features of aqueductal stenosis
dilated lat vent and 3rd vent normal 4th vent and CM
30
cerebellum and brain stem displaced inferiorly toward foramen magnum; effectively obliterating CM
arnold-chiari II malformation
31
arnold-chiari II malformation accompanies what NTD
myelomeningocele
32
enlargement of occipital horn of lat vent due to underdevelopment of surrounding brain tissues
colpocephaly 'empty head'
33
colpocephaly associated with __
agenesis of corpus callosum
34
maldevelopment of forebrain resulting in a range of ML cerebral and facial abnormalities
holoprosencephaly * forebrain = prosencephalon = cerebral hemispheres, thalami, hypothalamus
35
holoprosencephaly association
trisomy 13
36
causes for holoprosencephaly
inheritance TORCH gest DM
37
types of holoprosencephaly
alobar - no lobes, no horns semi lobar - some lobes, some horns lobar - most lobes, most horns * fused, dilated
38
absence of CSP, fused thalami, absent falx, ML facial defects
holoprosencephaly
39
ventriculomegaly characterized by near total or total absence of cerebral cortex
hydranencephaly (aka hydrancephaly) 'water filled head without brain'
40
which destructive cerebral lesion preserves vascularization of posterior fossa
hydranencephaly
41
cystic cavities within brain communicating with ventricles, subarachnoid space, or both
porencephaly 'passage within brain'
42
causes for porencephaly
infection, trauma, mat sickness, gest DM, FASD
43
clefts in fetal brain connecting the lat vents to subarachnoid space
schizencephaly 'splits in brain'
44
abnormal post fossa of the fetal brain accompanied by dilatation of 4th vent, enlarged CM, hypoplasia or agenesis of vermis
dandy-walker malformation
45
upward displacement of tentorium cerebelli (hiatus)
dandy-walker cyst
46
dandy-walker malformation association
trisomy 18
47
dandy-walker malformation vs. variant
variant = partial agenesis of vermis WITHOUT cystic dilatation of 4th vent
48
CM measurement
2-11 m mega CM considered a normal variant if vermis present
49
banana sign aka
'obliteration of CM' cerebellum pressing against occipital bone and absence of CSF in CM
50
obliteration of CM, banana sign, lemon sign =
arnold chiari II malformation
51
hypoplasia of cerebellum association
trisomy 18
52
AVF between enlarged vein of Galen and normal cerebral arteries
vein of galen malformation
53
vein of galen malformation association
cardiovascular dysfunction ie cardiomegaly
54
CSF filled sacs in subarachnoid space (adj to brain or spinal cord)
arachnoid cysts
55
failure of corpus callosum to develop association
dandy-walker malformation
56
thick, flat bundle of nerve fibres connecting the left and right cerebral hemispheres
corpus callosum allows for interhemispheric communication develops between 12-18w GA
57
CSP will not form if the __ doesn't
corpus callosum
58
periventricular calcifications are more commonly associated with __
fetal infection TORCH (esp cytomegalovirus)
59
low HC:AC high FL:HC
microcephaly
60
zika virus will cause
microcephaly among other issues
61
high HC:AC low FL:HC
macrocephaly
62
sono features of FASD
can be normal IUGR VSD, ASD facial abnormalities limb abnormalities
63
what facial defects can be detected from mid sagittal plane
frontal bossing proboscis flat/absent NB macroglossia micrognathia
64
what facial defects can be detected from coronal plane
cleft lip cebocephaly (one nostril) cyclopia hypotelorism/ hypertelorism etmocephaly cebocephaly
65
severe hypotelorism with proboscis-like nose and single nostril
cebocephaly
66
severe hypotelorism with arrhinia, proboscis ML and low set ears
ethnocephaly
67
which facial abnormality is associated with holoprosencephaly
ethnocephaly
68
median cleft lip association
trisomy 13
69
lethal skeletal dysplasia characterized by micromelia and macrocephaly with decreased thoracic circumference
thanotophoric dysplasia
70
macroglossia associated with which syndromes (2)
beckwith-wiedemann syndrome trisomy 21
71
micrognathia association
trisomy 13
72
nasal bone measurement
<2.5 mm