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54 Cards in this Set
- Front
- Back
look at ian suchet dvd
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normal face
frontal bossing cleft lip and palate nasal bone nasal proboscis |
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when is the fetal face identified sonographicallY? when can a fetal profile be seen?
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identified 10-12 wks
profile=13-14 wks |
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what are some causes of facial anomolies?
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-developmental/inherited
-affected by drugs/alcohol -chomosomal aberation |
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what drugs may affect facial developing?
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-alcohol
-codine -diazepam(valium) -retin A -antiepileptric drugs |
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what are some limitations for facial visualaization?
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-materal obesity
-fetal position -oligo |
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hyaloid artery
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visualized 16-30 wks
-echogenic line coursing from posterior globe through back of lens -regresses during pregnancy |
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what is the most valuble way of measuring the eyes?
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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.) |
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how far apart should orbits be? what does this indicate?
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should be separated by 1 globe w/ a general rule
-eye spacing abnormalities usually associated w/ other anomolies |
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when measuring orbits, how should they be seen?
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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)
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hypotelorism
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-decreased intraorbital distance
-assoc. w/ holoprosencephaly(most common) -associated w/ microcephaly, trisomy 21, and 13 -best scan plane=coronal oblique |
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hypertelorism
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-increased intraorbital distance
-may be isolated or part of a syndrome -assoc. anomolies: -craniosynostosis -anterior cephalocele -median cleft syndrome |
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name and explain some rare eye anomolies?
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-anopthalmia-absence of one or both eyes
-micropthalmia-abnormally small eyes -cataracts-abnormally echogenic lens -dacrocystocele-lacrimal duct cyst located inferomedial to orbit. |
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MEDIAN cleft face syndrome
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-aka frontal nasal dysplasia malformation complex
-hypertelorism -median clefting of the nose -varying degrees of palate cleftin -V shaped arterior hairline |
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Explin the embryology of the nose, eyes, and ears
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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 |
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fetal nose
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-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 |
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scanning criteria for nasal bone measurment
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-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` |
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diprosopus
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-duplication of craniofacial structures
-from isolated duplication to completer facial duplication -single neck and body -rare form of conjoined twins |
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otocephaly
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absence of eyes and forerain
-possible absence of mouth -incompatable w/ life |
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cyclopia
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-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 |
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cebocephaly
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-flat and rudimentry nose
-hypotelorism -single flat nostril -absent philtrum of upper lip -assoc. w/ holoprosencephaly |
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anopthalmia
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-congenital absence or severe hpoplasia of the eyes
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ethmocephaly
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-extreme hypotelorism w/ supraorbital proboscis or absent nose
-assoc. w/ holoprosencephaly |
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where is the proboscus seen with ethmocephaly, cebocephaly, and cyclopia?
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cyclo=most superior
ethmo=btw eyes cebo=most inferior |
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why is a cleft lip/palate devastating for newborns?
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because they can't feed becuase they will inhale the food.
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cleft lip and palate
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-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 - |
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what are the forms of cleft palate/lip
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-complete or incomplete
-unilateral/bilateral -symmetric/assymetric |
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unusual clefting may be the result of what?
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amniotic band syndrome
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what is the sonographic appearance of cleft lip?
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-anechoic region in the upper lip lateral to midline and extending into the nose
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what is hairlip(cleft lip) often associated w/
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club foot
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why should a thorough facial scan be done w/ polyhydramnios and a small stomach?
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because clefting may interfere w/ swallowing.
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what are some associated anomolies w/ cleft lip?
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-skeletal anomolies(most common)
-CVS-2nd common -trisomy13 -triploidy(69 chromosomes) -multiple syndromes -anencephaly -holoprosencephaly |
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when should tooth buds be seen by?
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-15/16 wks
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what should be done when scannign for facial clefts?
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-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) |
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macroglossia
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-enlarged tounge prenatally
-often protruding -beckwith-wiedemann syndrome -hypothyroidism |
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micrognathia(retrognathia)
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-shortening of the mandible
-small receeding chin -overbite -assoc. w/ trisomy 13 and 18 |
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prognathism
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large forward jutting jaw
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epignathus
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-rare pharyngeal tuor that arises from the palate
-extends through the mouth ad creats an anterior mass -caries greatly in size and texture |
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ears
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-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 |
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nuchal thickening
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-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% |
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fetal thyroid
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-functions by 12 wks
-thyroid enlargement or goiter may be seen with hypo/hyperthyroidism |
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goiter
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-thyroid enlargement
-impared swallowing=polyhdramions -may be seen w/ fetal hyper/ hypothyroidism -small percentage of mothers w/ grave's disease have hyperthyoid fetus |
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what are the fetal manifestations w/ a goiter?
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-IUGR
-oligo -tachycardia -polyhadramnios -hyperextension of the neck |
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what should mothers with thyroid disease be monitored for?
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-fetal goiters as it can be treated in utero
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cystic hygroma
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-aka nuchal cyst syndrom
-large septated nuchal fluid collection |
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give examples of giant neck masses
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-cervical teratomas
-orthopharyngeal |
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give examples of other neck masses
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--hemangioma
-lyphangioma -teratoma: these are all differentials for eachother |
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Micropthalmia
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abnormally small eyes
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cataracts
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appear as an abnorally echogenic lens
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Dacrocystocle
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lacrimal duct cyst located infromedial to orbit
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when scanning for facial clefts, what structures should be visialized
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-lips
-chin -alveolar ridge -nose -philtrum(midline groove of upper lip) |
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what are wourmian bones? Where are they located?
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Extra ossification center is identified btw frontal bones
If there is <3, they are called sutural bones. 36-8 |
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wourmian bones
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extra ossification center identified btw frontal bones
-<3=suteral bones -associated with wild chromosomal anomolies |
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describe the correct way to measure fetal nasal bone
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-midsagital profile
-image magnified -45 degree angle -must see equals sign, and tip of the nose - |
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what are some other possible neck masses?
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hemangioma
lyphangioma teratoma |