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54 Cards in this Set

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look at ian suchet dvd
normal face
frontal bossing
cleft lip and palate
nasal bone
nasal proboscis
when is the fetal face identified sonographicallY? when can a fetal profile be seen?
identified 10-12 wks
profile=13-14 wks
what are some causes of facial anomolies?
-developmental/inherited
-affected by drugs/alcohol
-chomosomal aberation
what drugs may affect facial developing?
-alcohol
-codine
-diazepam(valium)
-retin A
-antiepileptric drugs
what are some limitations for facial visualaization?
-materal obesity
-fetal position
-oligo
hyaloid artery
visualized 16-30 wks
-echogenic line coursing from posterior globe through back of lens
-regresses during pregnancy
what is the most valuble way of measuring the eyes?
OOD(outer orbital diameter)-because of the increased range of normal variation
-it may be used to date pregnancey when BPD cannot be measured
-useful when there is severe distortion of other biometric parameters(ie. cloverleaf skull, micromelia, etc.)
how far apart should orbits be? what does this indicate?
should be separated by 1 globe w/ a general rule
-eye spacing abnormalities usually associated w/ other anomolies
when measuring orbits, how should they be seen?
change axis until orbits appear the larges and the intraorbital distance is the greatest(can use transverse, coronal, or coronal oblique planes for measureing orbits)
hypotelorism
-decreased intraorbital distance
-assoc. w/ holoprosencephaly(most common)
-associated w/ microcephaly, trisomy 21, and 13
-best scan plane=coronal oblique
hypertelorism
-increased intraorbital distance
-may be isolated or part of a syndrome
-assoc. anomolies:
-craniosynostosis
-anterior cephalocele
-median cleft syndrome
name and explain some rare eye anomolies?
-anopthalmia-absence of one or both eyes
-micropthalmia-abnormally small eyes
-cataracts-abnormally echogenic lens
-dacrocystocele-lacrimal duct cyst located inferomedial to orbit.
MEDIAN cleft face syndrome
-aka frontal nasal dysplasia malformation complex
-hypertelorism
-median clefting of the nose
-varying degrees of palate cleftin
-V shaped arterior hairline
Explin the embryology of the nose, eyes, and ears
Nose-starts above the orbits as widely space entities(placodes) that move medialy and inferiorly
Eyes-start laterally and move medialy
-ears-start velow the mandible and move laterally and upward
fetal nose
-imaged coronally to visualize nares
-imaged midline sagital(profile) to measure nasal bone
-absence of nasal bone at 11-14 wks is associated w/ downs syndrome
-small or hypoplastic nose is seen w/ trisomy 18, apert's syndrome, de lange syndrome, and fetal toxins
scanning criteria for nasal bone measurment
-midline sagital profile
-magnify image to display only head and uppper thorax
-profle/transducer angle=45 degrees
-obtain 3 lines in nasal region
-=sign represents sline line, and nasal bone(inner)
-3rd line is tip of nose`
diprosopus
-duplication of craniofacial structures
-from isolated duplication to completer facial duplication
-single neck and body
-rare form of conjoined twins
otocephaly
absence of eyes and forerain
-possible absence of mouth
-incompatable w/ life
cyclopia
-single median orbit w/ various degrees of ocular fusion
-absent nose
-proboscus from lower forehead
-abscent facial bones
-absent philtrum of upper lip
-low set ears
-assoc. w/ holoprosencephaly
cebocephaly
-flat and rudimentry nose
-hypotelorism
-single flat nostril
-absent philtrum of upper lip
-assoc. w/ holoprosencephaly
anopthalmia
-congenital absence or severe hpoplasia of the eyes
ethmocephaly
-extreme hypotelorism w/ supraorbital proboscis or absent nose
-assoc. w/ holoprosencephaly
where is the proboscus seen with ethmocephaly, cebocephaly, and cyclopia?
cyclo=most superior
ethmo=btw eyes
cebo=most inferior
why is a cleft lip/palate devastating for newborns?
because they can't feed becuase they will inhale the food.
cleft lip and palate
-most common facial deformity at birth-lack of fusion of facial grooves
-fissure results in communication btw mouth and nasal cavity
-best visualized in coronal oblique
-incomplete cleft involves upper lip
-2/3 patiens w/ cleft lip have cleft palate
-congenital anomolies occur in more than 50% of fetuses w/ facial clefts
-
what are the forms of cleft palate/lip
-complete or incomplete
-unilateral/bilateral
-symmetric/assymetric
unusual clefting may be the result of what?
amniotic band syndrome
what is the sonographic appearance of cleft lip?
-anechoic region in the upper lip lateral to midline and extending into the nose
what is hairlip(cleft lip) often associated w/
club foot
why should a thorough facial scan be done w/ polyhydramnios and a small stomach?
because clefting may interfere w/ swallowing.
what are some associated anomolies w/ cleft lip?
-skeletal anomolies(most common)
-CVS-2nd common
-trisomy13
-triploidy(69 chromosomes)
-multiple syndromes
-anencephaly
-holoprosencephaly
when should tooth buds be seen by?
-15/16 wks
what should be done when scannign for facial clefts?
-frontal scans provide optimal view
-place transducer beneath chin, above forehead, or lateral to cheeks
STRUCTURES VISUALIZED:
-lips
-chin
-alveolar ridge
-nose
-normal philtrum(midline groove of upper lip)
macroglossia
-enlarged tounge prenatally
-often protruding
-beckwith-wiedemann syndrome
-hypothyroidism
micrognathia(retrognathia)
-shortening of the mandible
-small receeding chin
-overbite
-assoc. w/ trisomy 13 and 18
prognathism
large forward jutting jaw
epignathus
-rare pharyngeal tuor that arises from the palate
-extends through the mouth ad creats an anterior mass
-caries greatly in size and texture
ears
-rarly provide useful info
-low set ears=assoc w/ multiple syndromes
-look for gross deformities
-ears not always visualized due to:
-oligo
-fetal position
-maternal obesity
nuchal thickening
-thickening of skin on back of neck seen on the cerebellar veiw
->6mm@16-20wks=abnormal
-outer edge of bone to outer skin edge
-downs syndrome in 20-40%
fetal thyroid
-functions by 12 wks
-thyroid enlargement or goiter may be seen with hypo/hyperthyroidism
goiter
-thyroid enlargement
-impared swallowing=polyhdramions
-may be seen w/ fetal hyper/ hypothyroidism
-small percentage of mothers w/ grave's disease have hyperthyoid fetus
what are the fetal manifestations w/ a goiter?
-IUGR
-oligo
-tachycardia
-polyhadramnios
-hyperextension of the neck
what should mothers with thyroid disease be monitored for?
-fetal goiters as it can be treated in utero
cystic hygroma
-aka nuchal cyst syndrom
-large septated nuchal fluid collection
give examples of giant neck masses
-cervical teratomas
-orthopharyngeal
give examples of other neck masses
--hemangioma
-lyphangioma
-teratoma:
these are all differentials for eachother
Micropthalmia
abnormally small eyes
cataracts
appear as an abnorally echogenic lens
Dacrocystocle
lacrimal duct cyst located infromedial to orbit
when scanning for facial clefts, what structures should be visialized
-lips
-chin
-alveolar ridge
-nose
-philtrum(midline groove of upper lip)
what are wourmian bones? Where are they located?
Extra ossification center is identified btw frontal bones
If there is <3, they are called sutural bones. 36-8
wourmian bones
extra ossification center identified btw frontal bones
-<3=suteral bones
-associated with wild chromosomal anomolies
describe the correct way to measure fetal nasal bone
-midsagital profile
-image magnified
-45 degree angle
-must see equals sign, and tip of the nose
-
what are some other possible neck masses?
hemangioma
lyphangioma
teratoma