congenital vertebral anomolies Flashcards

1
Q

embygensis of vertebral bodies

A

come from paired somites that migrate during primary neurolation, sacrum and cocyx during secondary neurylation

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2
Q

how many chodification centers centers are there and when does that start

A

6th week and 3 pairs- one anterior and two posterior-

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3
Q

when does ossification begin

A

ninth embyonic and ends 14 to 18th week

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4
Q

which anomolies are defects in segmentation

A

block vertebae, unilateral bas, bar with hemivertebra

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5
Q

what are defects of formation

A

hemivertibrae, wedge

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6
Q

congential vertebral dislocation

A

superior getebra elogated posterior elements and large cana,

inferior mishapen with normal posterior elements

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7
Q

what is atlantal hemiring

A

bony discontinuit of C1 ring with lateral displacement of c1 lateral masses - occip con deformirty
sometimes absence of tranverse ligament- craniovertebral instability

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8
Q

segmental spinal dysgenesis

A

miltilevel spinal stenosis with hourglass shape of canal- absent pedicles, neurocentral jxn, and tp and involved lvevels
absent nerve roots at levels

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9
Q

medial spinal aplasia

A

3-11 thoracic and lumbar vertebraw suspended agensis without lumbrosacral agensis- budda like posture

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10
Q

what hemivertibra cause deformity and at what rate

A

isloated with disc above and below 2 degree a year in thoracic- a fused one cannot groe- incarcerated are ovoid with little growth potential

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11
Q

unilateral bar

A

potential 5 degress a year

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12
Q

scoliosis progress with which location

A

thoracolumbar as opposed to upper thoracic lesion

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13
Q

measure cobb angle

A

angles of most superior and inferior vetebrae

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14
Q

klippel-feil syndrome

A

segmentation anomalies- fused vertebrae, hemivertebaw, occipitlization of atlase

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15
Q

collegenopathies common anomolies

A

flat vertebral bodies, hoplatic dens, os odontoidem, atlantoaxial instability-35-60%

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16
Q

larson syndrome

A

FLNB gilamen B gene - coronal clefts in vertabae, subluxation of vertebae, atlantoaxial instability

17
Q

MURCS association

A

cervical and thoracic dysplasia associated with mullerian duct aplasia and renal agensis