Complications in Pregnancy Flashcards

1
Q

turner syndrome

A
  • 45 chromosomes, including a single X chromosome
  • elevated AFP
  • female fetus
  • 1:5000
  • cystic hygroma, cardiac defects, renal anomalies, cubitus valgus, short femur, general lymph edema
  • differential: cephalocele, trisomy 13, hydrops fetalis
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2
Q

beckwith-wiedemann

A
  • classic triad of macrosomia, omphalocele, and macroglossia
  • increases risk of developing wilms tumor, hemihypertrophy, renal anomalies,a nd hepatosplenomegaly
  • hemihypertrophy, macroglossia, omphalocele
  • differential: down syndrome
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3
Q

sequence

A

refers to a pattern of multiple anomalies that results from a single anomaly or mechanical factor

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4
Q

monochorionic/monoamniotic

A
  • two or more fetuses
  • single gestational sac
  • no membrane
  • zygote splits 10-14 days postfertilization
  • differential: technical difficulty in locating membrane
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5
Q

dichorionic/diamniotic

A
  • zygote splits within 3-5 days of fertilization
  • four-layered membrane
  • two or more individual gestational sacs and placentas
  • thick membrane with V shape called twin peak or lambda sign
  • differential: mirror image artifact
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6
Q

twin to twin transfusion syndrome

A
  • same sex fetuses
  • single placenta
  • arterial blood of the donor twin pumps into the venous system of the recipient twin
  • recipient twin ultimately receives too much blood
  • donor twim may display IUGR and oligo
  • receiving twin may aquire hydrops and poly
  • differential: acardiac twin or poli-oli syndrome
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7
Q

cubitus valgus

A

abnormal outward bending or twisting of the elbow

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8
Q

exencephaly

A

a condition where the skull is defective causing exposure or extrusion of the brain

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9
Q

disruption

A

is a defect of an organ resulting from the breakdown of previously normal tissue

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10
Q

hydrops fetalis

A
  • an abnormal interstitil accumulation of fluid in the body cavities and soft tissues
  • fluid accumulation may results in anasarca, ascites, pericardial effusion, pleural effusion, placentomegaly, and polyhydramnios
  • may result from antibodies in the maternal circualtion that destroythe fetal red blood cells or without evidence of clood group incompatibility
  • sonography cannot differentiate immune from nonimmune hydrops
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11
Q

multifetal gestations

A
  • 70% of pregnancies beginning with twins will deliver a singleton pregnancy
  • monozygotic twins results from a single fertilized ovum
  • dizygotic twins results from two separate ova
  • majority of pregnancies are dizgotic
  • dizygotic pregnancies are always dichorionic/diamniotic
  • twin A closet to the internal os
  • IUGR most common causediscordant growth in a dichrionic multifetal gestation
  • twin-twin transfusion syndrome is the most common cause of discordant growth in a monochrorionic multifetal gestation
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12
Q

chorionic villi sampling

A
  • performed between 10 and 12 gestational wks
  • results after 1 wk
  • identify masses
  • assess fetus postprocedure
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13
Q

limb body wall complex

A
  • rare complex malformation caused by the failure of closure of the ventral body wall
  • two or more defects
  • ventral wall defect, cranial anomalies, marked scoliosis, limb defects, short umbilical cord, amniotic bands
  • differential: amniotic band syndrome or trisomy 13
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14
Q

conjoined twins

A
  • monozygotic
  • fusion of twin fetuses
  • usually anterior and one body part
  • inseparable fetal bodies and skin contours, no membrane
  • differential: acardiac twin or normal twin pregnancy
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15
Q

amniotic band syndrome

A
  • ruptured amnion sticks and entangles fetal parts
  • associated with fetal abnormalities and amputations
  • thin hyperechoic linear structure floating within the amniotic cavity
  • feta abnormalities
  • differential: synechia, amniotic chorionic separation, limb-body wall complex, placetnal shelf
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16
Q

fetus papyraceus

A
  • demise of a twin that is too large to reabsorb
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17
Q

clinodactyly

A
  • inward curving of the fifth finger associated with Downs
18
Q

acardiac twin

A
  • rare
  • diamniotic/monochorionic
  • twin reversed arterial perfusion
  • blood shunted through a vein to vein and artery to artery
  • places a large cardiovascular burden on the normal twin
  • acardiac
    • poorly developed upper body, anencephaly, absent or poor heart, limbs may be present
  • normal
    • hydrops, poly, cardiac failure
19
Q

immune hydrops

A
  • rh sensitivity
  • scalp edema, pleural effusion, poly, placentomegaly
  • differential: nonimmune hydrops or pleural effusion
20
Q

eagle-barret syndrome

A
  • prune belly syndrome
  • hypotonic abdominal wall muscles
  • associated with dialted fetal bladder, small thorax, and imperforate anus
  • hydronephrosis, megaureter, oligo, small thorax, large abdomen, cryptorchidism, hip dislocation, scoliosis
  • differential: urinary obstruction or urethral atresia
21
Q

deformation

A

refers to an abnormal form, shape, or position of a part caused by mechanical forces antenatally

22
Q

spalding sign

A

overlapping of the crainal bones associated with fetal demise

23
Q

meckel-gruber syndrome

A
  • lethal condition
  • occurs equally in males and females
  • autosomal recessive
  • encephalocele, infantile polycystic renals, oligo, bladder not visualized, polydactyly
  • differential: trisomy 13 or infantile polycystic disease
24
Q

vanishing twin

A
  • early fetal demise of one embryo
  • twin pregnancy
  • demised twin resolves
  • becomes singleton pregnancy
  • differential: succenturine placenta or subchorionic hemorrhage
25
Q

edward syndrome

A
  • trisosmy 18
  • 80% of cases display a clenched fist
  • decrease in AFP
  • overall poor prognosis
  • female prevalence
  • heart defects, choroid plexus cysts, clenched hands, micrognathia, renal anomlaies, cleft lip and palate, omphalocele, two vessel cord
  • differential: trisomy 13 or triploidy
26
Q

anasarca

A

severe generalized massive edema often seen with hydrops fetalis

27
Q

stuck twin

A
  • poli-oli sequence
  • monochorionic/diamniotic
  • usuallyamnifests between 16 and 26 gestational weeks
  • one twin oligo, other twim poly
  • differential: acardiac twin, twin to twin
28
Q

triploidy

A
  • three complete sets of chromosomes
  • most will abort spontaneously
  • 1:5000
  • early onset IUGR, holoprosencephaly, hypertelorism, micrognathia, microphthalmia, ventriculomegaly, oligo, 2 vessel cord, cardiac anomalies, clubfeet, syndactyly
  • differential: trisomy 13 or 18
29
Q

embryoscopy

A
  • permits direct viewing of the developing fetus
  • assess fetus after procedure
30
Q

malformation

A

refers to a defect of an organ that results from an intrinsically abnormal development process

31
Q

cordocentesis

A
  • used to analyze fetal chromosomes
  • fetal blood is aspirated through the umbilical cord
  • assess fetus postprocedure
32
Q

amniocentesis

A
  • used to analyze fetal chromosomes in early pregnancy
  • typically between 15-18 wks
  • can be preformed as early as 12 gestational wks
  • recheck fetal well being after procedure
33
Q

patau syndrome

A
  • trisomy 13
  • 90% of cases display cardiac defects
  • syndrome of midline defects
  • 1:25,000
  • poor prognosis
  • holoprosencephaly, microcephaly, cystic hygroma, absent or small eyes, cardiac defects, omphalocele, polycystic kidneys, clubfoot, polydactyly, IUGR, poly, facial cleft
34
Q

sandal toe deformity

A

increased distance between the first and second toes associated with Downs

35
Q

eclampsia

A

gravest form of pregnancy induced maternal hypertension characterized by seiures, coma, proteinuria, and edema

36
Q

pentalogy of cantrell

A
  • congenital disorder characterized by two out of the following major defects
    • cardiac, abdominal wall defect, diaphragmatic hernia, defect of diaphragmaric pericardium, ectopia cordis
  • pulsating mass outside of the chest, ophalocele, gastroschisis
  • differential: beckwith-wiedemann or acardiac twin
37
Q

syndactyly

A

congential anomaly characterized by the fusion of the finger and toes

38
Q

nonimmune hydrops

A
  • large for dates
  • anasarca, edema, ascites, pleural effusion, pericardial effusion, poly, placentomegaly, fetal tachycardia, 200-240 bpm
  • differential: immune hydrops or pleural effusion
39
Q

down syndrome

A
  • trisomy 21
  • decrease in AFP
  • 1:800 live births
  • coexisting anomalies dicate overall prognosis
  • 30% of cases demonstrate duodenal atresia
  • nuchal fold >6mm, cardiac folci, macroglossia, low set ears, short stature, brachycephaly
  • differential: beckwith-wiedemann syndrome
40
Q

monochorionic/diamniotic

A
  • zygote splits 5-10 days after fertilization
  • three layer membrane
  • two or more individual gestational saces with shared placenta
  • membrane attachment of one chorion creates a T shape
  • moderately thick membrane
  • differential: mirror image artifact