Module 10.2 : Soft Markers Flashcards
1
Q
soft markers
A
- increase the fetal risk for a genetic disease
- correlation with other risk factors
+ history
+ maternal age over 35
+ maternal serum testing results - patients are referred for genetic counselling to review risk of having a chromosomally abnormal fetus
- patients decide if they will choose to have a genetic testing like an amniocenteses or CVS
2
Q
5 soft markers on ultrasound
A
- nuchal fold > 6mm
- echogenic bowel
- mild ventriculomegaly > 10 mm
- echogenic focus in the heart
- choroid plexus cysts
3
Q
3 soft markers when seen alone not with chromosomal abnormality
A
- single umbilical artery \+ cardiac abnormalities \+ renal abnormalities \+ growth restriction - enlarged cisterna magna > 10mm - pyelectasis \+ dilation of kidneys
4
Q
soft markers associated with trisomy 21
A
- EIF = echogenic intracrdiac focus
- thick nuchal fold
- echogenic bowel
- shortened femur/ humerus
- absent nasal bone
5
Q
echogenic intracardiac focus (EICF) (EIF)
A
- must be as bright as bone
+ 4 chamber splits screen
+ turn down gain all the way till bone disappears then notice if still present - 88% only in left
- 5% in right
- 7% in both
- right sided, biventricular, or multiple are reviewed
- NOT ASSOCIATED WITH CONGENITAL HEART DISEASE
6
Q
nuchal fold
A
- 16-17 6/7 weeks >/= 5mm
- 18-24 weeks >/= 6mm
- nuchal index
+ mean nuchal fold / BPD
+ value of 11
7
Q
echogenic bowel
A
- must be as bright as bone \+ same procedure as EIF - association with nonchromosomal abnormalities \+ cystic fibrosis \+ congenital infection \+ intra-amniotic bleed \+ Down syndrome
8
Q
shortened long bones
A
- femur or humerous
- below 2.5% fro gestational age
- > 0.9 of that predicted by measure BPD
- use BPD/long bone chart
9
Q
choroid plexus cysts
A
- CPCs
- demonstrate in 2 planes
- cyst >/= 3mm
- look for open hands
10
Q
fetal renal pelvic dilation
A
- not a marker on its own
- if seen with other markers then considered a multiple marker and more worrisome
- 16-20 wks >/= 5mm
- if > 10mm at any time in a pregnancy is a concern for renal blockage or hydronephroses
11
Q
2 vessel cord
A
- singel umbilical artery
- could result in
+ cardia
+ renal
+ low birth weight - fetal echo don’t at 24 wks
12
Q
mild ventriculomegaly
A
- > /= 10mm
- trisomy 21
+ idiopathic
= don’t know why they are connected
13
Q
nasal bone
A
- hypoplastic or absent nasal bone is big marker for T21
- routinely seen on nuchal lucency exam
- not routinely scanned in detailed but seen in profile
14
Q
what to assess for nasal bone
A
- absent or hypoplastic
- ethnicity must be considered
- Caucasian pop absent nasal bone is high risk for aneuploidy
- having a nasal bone significantly decreases risk of T21
15
Q
fifth finger clinodactyly
A
- hypoplastic or absent mid phalanx of fifth digit
- finger will curve inward
- marker for T21