ANOMALIES OF FETAL NECK, HEAD, & SPINE Flashcards

1
Q

ANOMALIES OF THE FETAL NECK, HEAD, AND SPINE AKA:

A

NEURAL TUBE DEFECTS

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2
Q

ABSENSE OF CEREBRAL HEMISPHERES AND OVERLAYING SKULL AND SCALP. (ALSO THE MOST COMMON CONGENITAL ANOMALY OF CNS)

A

ANENCEPHALY

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3
Q

WHAT IS PRESENT IN HALF THE CASES OF ANENCEPHALY?

A

POLYHYDRAMNIOS

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4
Q

WHAT IS THOUGHT TO BE CAUSED BY A BILATERAL BLOCKAGE OF THE INTERNAL CAROTID ARTERIES?

A

HYDRANENCEPHALY

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5
Q

TOTAL OR NEAR TOTAL ABSENCE OF CEREBRAL HEMISPHERES

A

HYDRANENCEPHALY

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6
Q

FAILURE OF PROSENCEPHALON (FOREBRAIN) TO DIVIDE INTO DOUBLE LOBES OF CEREBRAL HEMISPHERES, THALAMI ARE FUSED.

A

HOLOPROSENCEPHALY

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7
Q

WHAT ANOMALY HAS A SINGLE COMMON VENTRICLE THAT IS HORSESHOE SHAPED AND ASSOCIATED WITH CYCLOPIA AND PROBOSCIS

A

HOLOPROSENCEPHALY

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8
Q

FAILURE OF LIP FUSION PRIOR TO 35 DAYS FROM CONCEPTION.

A

FACIAL CLEFTS

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9
Q

CYSTIC AREA IN BACK OF THE BABIES HEAD; OBSTRUCTION OF HINDBRAIN

A

DANDY WALKER MALFORMATION

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10
Q

WHAT 4 ULTRASOUND CHARACTERISTICS WILL YOU SEE ON US W/DANDY WALKER MALFORMATION?

A
  1. CYSTIC ENLARGEMENT OF 4TH VENTRICLE
  2. DIALATED 3RD VENTRICLE
  3. VARIABLE DIALATION OF LATERAL VENTRICLES
  4. CEREBELLAR LOBES SPLIT APART AND ABNORMAL IN SHAPE.
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11
Q

BONY DEFECT IN CALVARIUM, W/HERNIATION OF BRAIN AND/OR MENINGES.

A

CEPHALOCELE (ENCEPHALOCELE)

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12
Q

WHAT IS ASSOCIATED W/POLYHYDRAMNIOS AND 80% OF THE TIME HYDROCEPHALUS IS PRESENT?

A

CEPHALOCELE (ENCEPHALOCELE)

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13
Q

ABNORMAL INCREASED/DIALATION DUE TO FLUID IN CEREBRAL VENTRICLES MOST COMMONLY SEEN W/SPINA BIFIDA

A

HYDROCEPHALUS

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14
Q

ARNOLD CHIARI MALFORMATION AKA

A

BUDD CHIARI MALFORMATION

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15
Q

COMMON TYPE OF HYDROCEPHALUS & ASSOC. W/SPINA BIFIDA; CEREBELLUM IS PULLED THROUGH CISTERNA MAGNA.

A

ARNOLD CHIARI MALFORMATION

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16
Q

“BANANA SIGN” - SHAPE OF CEREBELLUM
“LEMON SIGN” - NARROWER PORTION OF ANT PORTION OF HEAD
“BAT WING SIGN” - DIALATION OF LAT VENTRICLES, BILATERAL AND SEVERE

A

ARNOLD CHIARI MALFORMATION

17
Q

PATIAL ABSENSE OF CAVUM SEPTUM PELLUCIDUM (NORMALLY SHOULD POINT TO FRONT OF BABIES HEAD)

A

ARNOLD CHIARI MALFORMATION

18
Q

HC MEASURES >3 STANDARD DEVIATIONS BELOW NORMAL.

A

MICROCEPHALY

19
Q

ASSOC. W/TRISTOMY 18 5% OF THE TIME; BILATERAL CYSTS >10 MM HAVE HIGHER ASSOC. W/ABNORMAL KARYOTYPE

A

CHOROID PLEXUS CYSTS

20
Q

MAJORITY OF CYSTS IN BACK OF BABIES NECK; 80% ORIGINATE FROM POSTEROLATERAL PORTION OF NECK

A

CYSTIC HYGROMA

21
Q

ONLY SEEN IN GIRLS; ELBOW MALFORMATION

A

TURNERS SYNDROME

22
Q

DEFECT IN SPINE DUE TO LACK OF FUSION OF TWO HALVES OF VERTEBRAL ARCH

A

SPINA BIFIDA

23
Q

MOST COMMON SPINA BIFIDA LOCATION

A

LUMBAR SACRAL

24
Q

MENINGOCELE (SPINA BIFIDA)

A

ONLY MENINGES PROTRUDE

25
Q

MENINGOMYELOCELE (SPINA BIFIDA)

A

MENINGES AND SPINAL CORD PROTRUDE, CAN CAUSE PARALYSIS

26
Q

OCCULT SPINA BIFIDA

A

SMALL DEFECT W/NO PROTRUSION OF MENINGES OR CORD

27
Q

HIGH ASSOC. W/ARNOLD CHIARI MALFORMATION & ELEVATED SERUM ALPHA FETOPROTEIN LEVELS

A

SPINA BIFIDA

28
Q

CYST ARISING FROM THE VENTRICLE THAT DEVELOPS AS A CONSEQUENCE OF PARENCHYMAL HEMORRHAGE.

A

PORENCEPHALIC CYST

29
Q

DILATION OF VENTRICLES W/ACCUMULATION OF CEREBROSPINAL FLUID USUALLY DUE TO BLOCKAGE OF DRAINAGE PATHWAYS.

A

HYDROCEPHALUS (AKA VENTRICULOMEGALY)