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When is organogenesis
complete? 12 weeks

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When is the GB seen? 20 weeks

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Fetal GB

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Fetal GB
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Fetal GB

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What is suspected when the spleen is


enlarged in a fetus? Rh immunoIncompatibility

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When can the stomach be


seen? 14 weeks

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If the stomach is not seen by 16 weeks,


what could be the problem? esophageal atresia
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What is the stomach a landmark for? AC

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What does the intestines act as in utero? resevor for meconium

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peristalisis does not occur until birth

Why does the the fetus not poo in utero anal sphincter is closed

*unless in distress

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kidney / testis crisscross no data


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amniotic fluid + fetal cells


what is meconium made of
bacteria and enzymes added

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spleenomegaly

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Pancreas

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What is the size of the adrenals in a 20x larger in fetus than adults
fetus? can mimic kidneys
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adrenal

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adrenal

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______________ is directly proportional to


AC. liver size

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What is hypoxic? pertaining to low oxygen


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What does the umbilical arteries


become after birth? hypogastric ligament

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What does the umbilical vein become


after birth? ligament venosum

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What measurements do we take


AC
involving the abdomen?
renal length

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trans spine - 3 oss center

What is the AC landmarks? J - portal vein

stomach & GB
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What is esophageal atresia? congenital atresia of the esophagus

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What causes esophageal failure of recanalization of the GIT


atresia? a blind end tube is result

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What is present in most cases of


esophageal atresia? tracheo-esophageal fistula

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What percent of esophageal atresia


have a tracheo-esophageal fistula 90%
present?
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What is the sonographic appearance of polyhydramnios


esophageal atresia? stomach usually not identified

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Duodenal atresia

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What is duodenal atresia usually


associated with? Downs syndrome

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What is the sonographic appearance of Double bubble


duodenal atresia? polyhydramnios
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Duodenal atresia

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Double bubble

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When can duodenal atresia be


seen? 24 weeks

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tracheo-esophageal fistula
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duodenal atresia

duodenal stenosis
What causes a double bubble?
annular pancreas

jejunal atresia

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extension of pancreas tissue around


duodenal
What is an annular pancreas?
forming a ring

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What problems does annular pancreas feeding problems


cause in infants? reflux and vomiting

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What is the sonographic appearance of


bowel proximal to the blockage dilated
jejunal atresia?
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meconium ileus
What is the first sign of cystic fibrosis?
echogenic bowel

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meconium ileus

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meconium ileus

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small bowel disorder, presense of thick


meconium in the distal ileum
What is a meconium ileus?
impaction of abnormal thick sticky
mecomium
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Meconium Peritonitis

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Meconium Peritonitis

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Meconium Peritonitis

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What can obstructed bowel


perforation and infection
cause?
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What is the sonographic appearance of


meconium ileus? echogenic small bowel

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When is the migration of the kidney to


the abdomen complete? 9 weeks

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What causes pelvic kidneys? can be physical or hormonal

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What are horseshoe kidneys? inferior portion fuses early on


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When should the kidneys and the


bladder be seen? 15 weeks

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bubble sign

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When should the renal cortex and


medulla be differentiated? 25 weeks

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bubble sign
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Cross-over fusion kidneys

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What happens with bilateral renal olighydramnios usuually resulting in


agenesis? miscarriage - always fatal

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What is Potter's type 2? multicystic dysplastic kidneys

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Urachal fistula
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Urachal fistula

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Urachus doesn't close and belly button


What is a urichal fistula? leaks urin

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Urachal cyst

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Urachal cyst
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Unilateral renal agenesis

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Mesoblastic Nephroma AKA: fetal renal


harmatoma & congenital Wilm's tumor

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Mesoblastic Nephroma AKA: fetal renal


harmatoma & congenital Wilm's tumor

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Wilm's Tumor AKA:


Nephroblastoma
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Congenital Wilms' tumors

What is mesoblastic big benign mass usually expresses its self by 3 months

nephroma? most common neonatal solid tumor

mostly in boys

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What is Nephroblastoma? wilms tumor

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What is the most common malignant


tumor of childhood? Wilms tumor

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At what age does wilms tumor usually


occur? commonly occurs at 3 yrs
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a fibrous cord that extends from the


what is a Urachus? umbilicus to the bladder.

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Severe oligohydramnios
What is the sonographic appearance of
Absent kidneys
Potter's type 2?
Nondistended bladder

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disorder associated with multiple


What is IPKD? bilateral cysts

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Infantile Polycystic Kidney Disease


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Infantile Polycystic Kidney Disease

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What is another name for


IPKD? Potter Type 1

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Urachal cyst

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Is IPKD recessive of dominant? recessive


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Perinatal – renal failure in utero

Neonatal
What are the 4 groups of IPKD?
Infantile

juvenile

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When does neonatal IPKD


within 1st month after birth
occur?

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When does infantile IPKD


occur? 3 - 6 months

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When does juvenile IPKD


occur? 1 - 5 years
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enlarged

hyperechoic

What is the sonographic appearance of homogeneous hyoerechoic large kidneys

IPKD? increased kidney AC

small bladder

loss of corticomedullary differentiation

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1. polucystic kidneys
What is Meckyl-Gruber 2. posterior
syndrome? encephalocoele/holoprosencephaly
3. polydactyly

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large
What is adult polycystic kidney disease?
echogenic

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What age does APKD usually


age 30 with hypertension
occur?
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If one person has APKD what is the


chance of passing it on to children? 50%

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What is polycystic kidney auto dominant


disease? family history

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disorder associated with unilateral cystic lesions

correspond to dilated collecting tubules

What is multicystic dysplastic kidneys? Enlarged

unilateral

nonfunctioning

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Bilateral multicystic dysplastic kidney


disease
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unilateral multicystic dysplastic kidney


disease

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unilateral multicystic dysplastic kidney


disease

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What happens to the contralateral


kidney with MDK? enlarges to compensate

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multiple, round

various sizes
What is the sonographic appearance of
bladder not seen
bilateral MDK?
olighydramnios

Poor Prognosis
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multiple, round

What is the sonographic appearance of various sizes


unilateral MDK? bladder seen

hydronephrosis

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What is UPJ? uritopelvis junction

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What is UVJ? uritovesicilar junction

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Hydronephrosis
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Where is a double collecting system


most likely to have hydro? the superior collecting system

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What is the most common fetal


anomaly? hydronephrosis

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What is hydronephrosis usually caused


by? UPJ or UVJ obstruction

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What is a UPJ obstruction caused by? bend or kink in ureter


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What is a UVJ obstruction caused by? bad valves at trigone region

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What do normal ureters


measure? 1 mm

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Prune belly syndrome usually occurs in


_____________ boys

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Dilation of the renal pelvis due to


What is hydronephrosis? blockage
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Pyelectasis

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abnormal collection of urine within the


What is pyelectasis? renal pelvis 5-9 mm

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Caliectasis

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Caliectasis
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rounded calyces with renal pelvis


What is calyectasis? dilatation

front 114 Rare congenital abnormality. A partial or complete lack of abdominal


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wall muscles w/ renal abnormalities. Usually in males.

anterior abdominal wall defect

urinary tract obstruction

What is Prune Belly cryptorchidism

Syndrome? hypoplastic abdominal wall muscles

massive distention of bladder

wrinkling

urethral obstruction

bladder enlarges
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Prune Belly

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Prune Belly
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What is another name for prune belly


syndrome? Eagle Barrett syndrome

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hydronephrosis with echogenic renal parenchyma

oligohydramnios
What is the sonographic appearance of urinary ascites
prune belly syndrome
a dystrophic bladder

peritoneal calcifications

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Obstruction of the urinary outflow. Can be acquired or


congenital.
What is ureteropelvic junction obstruction at the confluence of the kidney and the
obstruction? ureter

Sporadic

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What is the most common cause of


hydronephrosis in neonates? UPJ obstruction
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UPJ obstruction

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UPJ obstruction

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will often show a dilated renal pelvis

What is the sonographic appearance of Doppler: Kidney w/higher resistive


ureteropelvic junction obstruction? indices

hyperechoic kidneys

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Obstruction of the uretrovesical junction causing urine


What is Ureterovesicle junction to back up into the ureters and kidneys.
obstruction? results from stenotic ureteral valve or fibrosis
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What is the sonographic appearance of megaureter


Ureterovesicle junction obstruction? hydronephrosis

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Ectopic ureterocele

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the distal ureter does not insert into the urinary bladder

Congenital cystic dilatations of the terminal submucosal


ureter
What is a Ectopic ureterocele?
surgical repair or can lead to loss of function

bad insertion of ureter into trigone region

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What is the sonographic appearance of Echogenic thin-walled cyst-like


a Ectopic ureterocele? structures within the bladder
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What is ectopic ureterocele usually


associated with? UVJ obstruction

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Posterior urethral valve

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most common congenital obstructive


lesion of the urethra
What is Posterior urethral valves?
congenital folds act of male urethra act
as valves to obstruct excretion

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marked distention bladder

hydronephrosis
What is the sonographic appearance of hydroureter
Posterior urethral valves?
oligohydramnios

keyhole sign
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Posterior urethral valve

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What is a keyhole sign? no data

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baby can't urinate

leading to
What is the major concern for babies olighydramnios
with posterior urethral valves?
pulmonary hyperplasia

risk of bladder rupture causing urinary ascites

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What is the most common cause of


death for fetus with posterior urethral pulmonary hyperplasia
valves?
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The cloaca is a structure in the development of the


urinary and reproductive organs.

plays a developmental role in

What is cloaca? genitals

bladder

rectum

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Bladder exstrophy

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What is the most severe form of bladder cloacal extrophy


exstrophy? colon is affected

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Testicular hydrocele
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Testicular hydrocele

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process vaginalis does not close


What causes a testicular hydrocele? completely causing abdominal
secretions in scrotal sac.

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Many testicular hydroceles _____________ Many testicular hydroceles heal themselves within 24
within ____________. months.

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What week do the testicles descend? 28 weeks


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congenital anomaly, protrusion of the


What is Bladder exostrophy? urinary bladder through a defect in the
abdominal wall.

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soft-tissue mass protruding through


abdomen
WHat is the sonographic appearance of
Bladder exostrophy? absence of urinary bladder

separation of pubic bone

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What is a differential diagnosis of


bladder exostrophy? gastroschisis or omphalocele

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fluid-filled sac surrounding a testicle


What is a Testicular Hydrocele?
usually benign
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What is the sonographic appearance of simple fluid collection surrounding the


Testicular Hydrocele? testis.

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general term for a disorder of the development of bone


and cartilage
What is Osteochondrodysplasia? hard to identify prenatally

* filler in multiple choice...usually missed by U/S

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Explain the TC of a fetus with


Osteochondrodysplasia? measure small

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red flag
What should you do if the femur
marker for trisomy 21
measures small?
measure humerus
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What is the key bone


measurement? femur length

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When do the long bones begin to end of embryonic period


ossification? week 12

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What is TC? thoracic circomuference

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mandible & clavicle


What are the first bones to ossify?
Week 8
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polyhydramnios
what usually occurs with
fetal structural anomalies
musculoskeletal abnormalities?
family history of recurrent syndrome

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Why are the most lethal musculoskeletal


anomolies easier to identify? they have severe presentations

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carpal

metacarpal

What bones can be Acromelia? tarsels

metatarsels

phalanges
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Acromelia
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Acromelia

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Bone abnormality shortening of distal


What is Acromelia?
limb segment.

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Acromelia

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Mesomelia
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shortening of middle limb


What is Mesomelia?
segment.

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tibia

fibula
What bones can be Mesomelic ?
ulnar

radius

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What is Rhizomelic shortening? Shortening of proximal limb segment

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Rhizomelia
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Rhizomelia

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femur
What bones can be Rhizomelic ?
humerus

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Shortening of proximal and distal limb


What is Micromelia shortening? segment

dwarfism

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What is Extactyly? Absence of fingers or toes


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Hemimelia

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What is Hemimelia? Absence of below elbow or knee

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Phocomelia

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Phocomelia
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Phocomelia

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Absence of middle segment


What is Phocomelia? foot and hand would be attached to
femur and humerus

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fusion of legs
What is Sirenomelia?
mermaid syndrome

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Sirenomelia
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Sirenomelia

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Sirenomelia

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Absence or malformation of individual


What is Dystoes? bones

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What is Arthrogryposis? rigid extremities


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What is the possible cause of


Arthrogryposis? olighydramnios

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joint contractures and rigidity.

head was severely hyperextended

What is the sonographic appearance of fixed extremities

Arthrogryposis? flexed arms

clubbed feet

clenched hands

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What is Polydactyly? extra fingers or toes.

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Polydactyly
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Polydactyly

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Clinodactyly & club foot

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Clinodactyly

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What is Clinodactyly? curvature of a digit


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What is Pterygium? webbing across joints

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Pterygium

webbing across joints

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Talipes equinovarus

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Talipes equinovarus
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Ectrodactyly

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Ectrodactyly

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AKA Club foot.


What is Talipes? front half of the foot turns inwards and
downwards

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prominent calcaneus and a convex


rounded bottom to the foot. The foot
What is Rocker-bottom feet? resembles the bottom of a rocking chair.

marker for trisomy 18


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Rockerbottom feet

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Thanatophoric dysplasia

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Thanatophoric dysplasia

achondrogenesis
What are the lethal forms of Skeletal
camptomelic dysplasia
dysplasia?
osteogenesis imperfectal - Type II

Sirenomelia
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What is the most common non-lethal


bone dysplasia? achondroplasia
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Achondroplasia

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by femur length

When can rhyzomelia be diagnosed in 27 - 30 weeks


utero?
measurement of femur length starts
dropping off

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What are the Non-lethal forms of achondroplasia


Skeletal dysplasia? osteogenesis imperfecta Type IV

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severe skeletal disorder characterized by extremely


short limbs and folds of extra skin on the arms and legs.

rhizomelia
What is Thanatophporic Dysplasia? bowed long bones

narrow thorax

large head
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What is the most common form of lethal Thanatophporic Dysplasia


dwarfism? causes severe micromelia

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clover leaf skull

narrow chest

short ribs
What is the sonographic appearance of underdeveloped lungs
Thanatophporic Dysplasia?
enlarged head

large forehead and

prominent, wide-spaced eyes.

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Kleeblattshadels

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Kleeblattshadels
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What is another name for cloverleaf


skull? kleeblattschädel

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horseshoe

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cloverleaf skull

What are associated anomolies of horseshoe kidneys


Thanatophporic Dysplasia? ASD

imperforate anus

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Achondrogenesis
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What is the second most common form


Achondrogenesis
of lethal dwarfism?

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rare lethal form of short limbed


dyplasia
What is Achondrogenesis? severe malformation of bones and
cartilage. Babies usually still born or die
shortly

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What are the two types of no data


Achondrogenesis?

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demonstration of the triad

What is the sonographic appearance of severely shortened limbs

Achondrogenesis? lack of vertebral ossification

large head with slightly decreased ossification


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Camptomelic Dysplasia: bowing of the


What is Camptomelic Dysplasia?
long bones

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tibia
What are the most common bones
affected by Camptomelic Dysplasia?
femur

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bowing of long bones


What is the sonographic appearance of
hydrocephalus
Camptomelic Dysplasia?
hydronephrosis

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heart disease
What are the anomolies associated with
hydrocephalus
Camptomelic Dysplasia?
hydronephrosis
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early disruption of caudal portion of the


neural tube
What is caudal regression syndrome
caused by? (sacral anomolies)

includes a range of anomolies

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fusion of the lower extremities


What is caudal regression syndrome?
male prevalence 3:1

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What is a mild case of caudal


regression syndrome? sacral anomalies

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What is the most severe form of caudal


regression syndrome? Sirenomelia
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Caudal regression syndrome

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What are the associated anomalies of diabetes


caudal regression syndrome? monozygotic twins

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AKA Mermaid Syndrome, very rare


Sirenomelia congenital deformityin which the legs
are fused together

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disorder of production, secretion or


What is Osteogenesis Imperfecta Type function of collagen
II?
most severe form
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Osteogenesis Imperfecta type 2

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What is Osteogenesis Imperfecta Type bone fragility caused by


II characterized by? hypominerization

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What can delivery trauma lead to with intracranial hemorrhage


Osteogenesis Imperfecta Type II? stillbirth

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AKA Brittle bone


What is Osteogenesis Imperfecta Type
fractured or bowed
IV?
demineralization of bone
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Whe does Osteogenesis Imperfecta can occur in 3rd trimester


Type IV occur? usually does not present until after birth

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decreased echogenicity

What is the sonographic appearance of fractures


Osteogenesis Imperfecta Type IV? cortical bone thinning

excessive trabecular bone transparency

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very short limbs and sometimes a face


What is Achondroplasia?
that is small in relation to the skull

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Anal atresia

Cardiac defects
What is VACTERL?
TracheoEsophageal atresia

Renal anomalies

Li b li
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vacterl

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Esophageal atresia

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How many anomalies need to be


present to be considered VACTERL? 3

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