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72 Cards in this Set

  • Front
  • Back

Most common neural tube defect?


Which gender has higher dominance?

Anencephaly / Aprosencephaly / atelencephaly.


Females.

What mimics acrania?


What’s the sono appearance of acrania?

Hypophosphatasia, osteogenesis imperfecta. (Hypomineraliztion of the cranium.)


Mickey Mouse appearance.

Meninges or meninges and brain herniate through a defect in the calvarium?


Most commonly involved in what part of the skull?

Cephalocele


Occipital bone most commonly

Spina bifida occurs at which regions?

Lumbar and sacrum regions

Gives cerebellum a banan shaped appearance. Leads to obliteration of cisterna magna. What’s this finding?

Arnold Chiari II malformation.

Is the skull has a strawberry sign associated with?


Lemon shaped skull is not specific to _________, but also to?

Trisomy 18.


Not specific to Spina Bifida. Can be for other CNS abnormalities: Encephalocele or non CNS Thanatophoric dysplasia.

Fetus has hypotelorism combined with normally placed nose and single nostril... what is this finding?

Cepocephaly

Fetus has hypotelorism combined with normally placed nose and single nostril... what is this finding?

Cepocephaly

Severe hypotelorism with probiscis superior to eyes. Facial clefts might be present. What’s the finding?

Ethmocephaly

Fetus has hypotelorism combined with normally placed nose and single nostril... what is this finding?

Cepocephaly

Severe hypotelorism with probiscis superior to eyes. Facial clefts might be present. What’s the finding?

Ethmocephaly

Hypotelorism with small eyes is associated with?


Holoprosencephaly is seen with other findings such as?

Trisomy 13.


Other sono findings seen w/ Holoprosencephaly is polyhydramnios, IUGR, microcephaly, hydrocephaly, omphalocele, cardiac defects, spina bifida, trisomy 13.

Hypotelorism with small eyes is associated with?


Holoprosencephaly is seen with other findings such as?

Trisomy 13.


Other sono findings seen w/ Holoprosencephaly is polyhydramnios, IUGR, microcephaly, hydrocephaly, omphalocele, cardiac defects, spina bifida, trisomy 13.

There is an absent Corpus callosum, absent CSP, what’s this potential finding?


What are factors that can cause this?

Agenesis of corpus callosum.


Factors: maternal Diabetes, alcohol, infection

Hypotelorism with small eyes is associated with?


Holoprosencephaly is seen with other findings such as?

Trisomy 13.


Other sono findings seen w/ Holoprosencephaly is polyhydramnios, IUGR, microcephaly, hydrocephaly, omphalocele, cardiac defects, spina bifida, trisomy 13.

There is an absent Corpus callosum, absent CSP, what’s this potential finding?


What are factors that can cause this?

Agenesis of corpus callosum.


Factors: maternal Diabetes, alcohol, infection

There’s an obstruction, atresia or stenosis of the aqueduct of sylvius?


What would you identify if this was happening?

Aqueductul stenosis.


Ventriculomegaly.

Choroid plexus cysts are associated with?


What should a sonographer evaluate?

Trisomy 18.


Eval hands and heart. Is there abnormal posturing, or polydactyl. Eval nasal bone, Nuchal fold, kidneys.

This contains cerebrospinal fluid and cellular debris that are trapped in neuroepithelial folds, what is the finding?

Choroid plexus cysts. Ventricles enlarged.

This contains cerebrospinal fluid and cellular debris that are trapped in neuroepithelial folds, what is the finding?

Choroid plexus cysts. Ventricles enlarged.

Cystic space as irregular shape possibly midline and posterior superior to third ventricle; turbulent flow.. what’s this finding?


Don’t confuse with?

Vein of Gallen Aneurysm.


Arachnoid cysts. (No blood flow in the structure).

This contains cerebrospinal fluid and cellular debris that are trapped in neuroepithelial folds, what is the finding?

Choroid plexus cysts. Ventricles enlarged.

Cystic space as irregular shape possibly midline and posterior superior to third ventricle; turbulent flow.. what’s this finding?


Don’t confuse with?

Vein of Gallen Aneurysm.


Arachnoid cysts. (No blood flow in the structure).

Arachnoid cysts differential?

Porencephalic cyst. No blood flow and cyst communicates with the ventricle (ventricular system).


Arachnoid cyst: no blood flow in the structure (Benign).

For cleft lip what’s the worse prognosis?

Bilateral open lip

For cleft lip what’s the worse prognosis?

Bilateral open lip

Sonographically: Fluid filled cleft in cerebral cortex extending from ventricle to calvarium. Ventriculomegaly seen and associated with absent CSP and corpus callosum. What’s the potential finding?

Schizencephaly

There’s an occlusion of internal carotid arteries, destruction of cerebral hemispheres, what’s the finding?

Hydranencephaly

There’s an occlusion of internal carotid arteries, destruction of cerebral hemispheres, what’s the finding?

Hydranencephaly

How to differentiate hydrocephalus from hydranencephaly?

Hydrocephaly - in tact falx and surrounding rim of parenchyma.


Hydranencephaly: Absent / partial absent falx

Ventriculomegaly seen, enlarged fetal head, what’s this finding?

Hydrocephaly

Ventriculomegaly seen, enlarged fetal head, what’s this finding?

Hydrocephaly

What are causes of Ventriculomegaly?

Spina bifida, encephalocele, DWM, agenesis of corpus callosum, Holoprosencephaly, thanatophoic dysplasia, achondroplasia, Schizencephaly, congenital infection.

Ventriculomegaly seen, enlarged fetal head, what’s this finding?

Hydrocephaly

What are causes of Ventriculomegaly?

Spina bifida, encephalocele, DWM, agenesis of corpus callosum, Holoprosencephaly, thanatophoic dysplasia, achondroplasia, Schizencephaly, congenital infection.

Fetal head has small BPD, small HC, small AC, sloping forehead. What’s the finding?


What is linked?

Microcephaly.


Teratogens linked, cytomegalovirus, toxoplasmosis, congenital infection, rubella.

Microcephaly is associated with?

Schizencephaly, Holoprosencephaly, craniosynostosis, trisomy 13, 18, 21, triploidy, Meckel Gruber Syndrome.

What is the characteristics of the meckel gruber syndrome?

Triad includes encephalocele, polydactlyl, bilateral dysplastic cystic kidneys.

What is the characteristics of the meckel gruber syndrome?

Triad includes encephalocele, polydactlyl, bilateral dysplastic cystic kidneys.

What is the biggest anomaly of face and neck?

Cleft lip/ palate

What is the characteristics of the meckel gruber syndrome?

Triad includes encephalocele, polydactlyl, bilateral dysplastic cystic kidneys.

What is the biggest anomaly of face and neck?

Cleft lip/ palate

Which plane to best visualize the orbits, nose, lips, tongue?


Which plane is the best to visualize orbit, nose, lip, maxilla, anterior portion of mandible?

Axial


Coronal

What is the clover leaf appearance suggest?

Craniosynostosis

This can be found anywhere on the fetal body and has internal blood flow?


These can be found on any organ. Vary in size, more echogenic that the placenta and homogenous. They are well defined, vascular. What’s this finding?


Which plane to best visual the lips?

Teratoma.


Hemangioma.


Coronal plane

What’s the common cause of macroglossia?

Beckwith Weidman Syndrome

What’s the common cause of macroglossia?

Beckwith Weidman Syndrome

Abnormal chin?


Single nostril finding called?


Finding includes hanging above the orbits or between the eye orbits?

Micrognathia.


Cebocephaly


Proboscis

What is interocular orbit?


What is binocular distance?


What’s ocular diameter?

Interocular orbit is measurement of medial wall of one orbit to the other medial wall of other orbit.


Binocular distance: measurement between lateral orbital rims.


Ocular diameter is measurement from medial wall to lateral one orbit.

If the third ventricle is identified what does this mean?


What’s the landmarks?

Won’t see unless dilated.


Landmark: third ventricle is between the right and left thalamus.

The BPD is at what level?

The CSP, thalamus, third ventricle, lateral ventricles

If you identify dangling choroid plexus this is associated to?

Spina bifida, chromosomal abnormality- Trisomy 21: Down Syndrome.

If there’s no other abnormalities identified with ventriculomegaly, this is isolated and can mean what?


What produces cerebrospinal fluid?


Landmarks of 4th ventricle?

Congenital infection.


Choroid Plexus.


Between the brain stem and cerebellum.

AFP levels peak at what gest age?


Cranial vault filled with fluid, partial falx, no cortex. No color in MCA. Absent cerebral hemispheres. What’s the finding?

16-18 weeks.


Hydranencephaly.

This connects two cerebral hemispheres?

Corpus callosum

This is noncommunicating hydrocephaly. Ventricular system can’t communicated without each other. What’s this finding?

Aqueductal stenosis

Defect of protrusion of meninges?


Closed defect- covered by hair or skin?


Commonly meninges and neural elements protrude via the defect?


Neural tube fails to close and meninges might protrude?

Meningocele.


Closed defect: covered by hair or skin- spina bifida occulta.


Meningomyelocele.


Spina bifida.

For neural tube pathology, Diabetes can cause?

Sirenomelia, mermaid syndrome, or missing sacrum.

Absent CSP, elevated third ventricle, interhemispheric cyst, what’s the finding?

Agenesis of corpus callosum

1. Simple: Tonsil herniation, 2. part of brain deformed- banana cerebellum. 3. Most complex; occipital encephalocele associated with hydrocephaly. What’s the finding?

Arnold Chiari Malformation

What’s the difference between communicating and noncommunicating?

Communicating is when outside ventricular system.


Noncommunicating is when it’s inside the ventricular system.

Increased Nuchal translucency, abnormal first trimester screen, abnormal quad screen, what could this be?

Trisomy 21, Down Syndrome

Increased Nuchal translucency, abnormal first trimester screen, abnormal quad screen, what could this be?

Trisomy 21, Down Syndrome

Clenched hands, rocker bottom feet, abnormal quad screen.

Trisomy 18- Edwards Syndrome

Increased Nuchal translucency, abnormal first trimester screen, abnormal quad screen, what could this be?

Trisomy 21, Down Syndrome

Clenched hands, rocker bottom feet, abnormal quad screen.

Trisomy 18- Edwards Syndrome

Hypotelorism, polydactyly, single umbilical artery?

Trisomy 13- Patau Syndrome

Increased Nuchal translucency, abnormal first trimester screen, abnormal quad screen, what could this be?

Trisomy 21, Down Syndrome

Clenched hands, rocker bottom feet, abnormal quad screen.

Trisomy 18- Edwards Syndrome

Hypotelorism, polydactyly, single umbilical artery?

Trisomy 13- Patau Syndrome

Fetal tachycardia identified, short femur, increased NT in 1st trimester?

Turner Syndrome

Fluid filled sac, but no embryo developed, what’s this finding?

Pseudo Sac