Fetal Genitourinary System Flashcards
The fetal kidneys develop within the pelvis and ascend into their normal position by:
9 weeks
By week ____ fully functional kidneys exist.
10
If kidneys fail to ascend into the normal position, they are most often located :
within the pelvis
Most common renal anomaly is the :
duplex collecting system
The kidneys can be sonographically identified as early as :
11-12 weeks
The gonads develop in the _______
upper fetal abdomen and descend into the pelvis
The testicles move down into the scrotum during ____ month of gestation.
7th
The fetal bladder can be seen as early as:
12 but should always be seen by 15 weeks
The urinary bladder normally fills and empties once every :
30 - 45 mins
VACTERL stands for:
vertebral, anal atresia, cardiac anomalies, tracheoesophageal fistula or esophageal atresia, renal anomalies, limb anomalies
Patients are considered to have VACTERL association if:
3 organs systems involved have abnormalities
Renal abnormalities are the most frequent cause of :
oligohydramnios
Urine comprises the greater part of the amniotic fluid after:
14 weeks
failure of a kidney to form:
renal agenesis
Sonographic finding when the kidney is absent in the abdomen, the adrenal gland can be noted in a parallel flattened position, sonographically known as:
“lying down” adrenal sign
When there is an absence of the kidney, and you place color doppler over the renal artery branches of the aorta there will be:
no identifiable renal artery branches
Bilateral renal agenesis, aka:
potter’s syndrome
Non-visualization of the urinary bladder and kidneys, with oligohydramnios, are considered a consistent finding with:
bilateral renal agenesis
Before making the conclusion of unilateral renal agenesis, the sonogrpaher should always analyze the:
fetal pelvis for a pelvidc kidney
In presence of unilateral renal agenesis, the contralateral kidney will :
enlarge, a condition known as compensatory hypertrophy
In order for an autosomal recessive disease to be passed to the fetus,
both parents must be carriers of the disease.
In the case of autosomal dominant disease how many parents must be the carrier(s) of the disease with the gene being dominant, in order to pass it to the fetus:
one
The typical sonographic findings of a fetus affected by ARPKD:
bilateral enlarged, echogenic kidneys, non detectable urinary bladder, and oligohydramnios
Condition associated with ARPKD which is a fatal disorder that is associated with renal cystic disease, occipital cephalocele, and polydactyly
meckel gruber syndrome
Fetuses with trisomy ____ and trisomy ____ may also have polycystic kidney disease.
13, 18
Cysts with ARPKD are:
microscopic
Cysts are not identifiable in ARPKD but are evident in:
multicystic dysplastic kidney