ortho conditions in childhood Flashcards

(72 cards)

1
Q

average child usually sits by what age

A

9 months

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2
Q

average child usually stands by

A

1 year

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3
Q

average child usually walks by

A

20 months

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4
Q

by what age are most cases of genu varum and valgum normally corrected

A

age 7

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5
Q

causes of in-toeing

A

femoral neck anteversion
tibial torsion
abnormal forefeet

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6
Q

femoral neck ante version means the femur can be ? rotated a lot

A

internally rotated a lot

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7
Q

is tibial torsion a normal variation

A

yes and should be ignored

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8
Q

surgery to correct abnormal forefeet should not be considered until after age ?

A

7

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9
Q

is flat foot normal variation

A

yes

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10
Q

most types of flat foot are ?

A

mobile

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11
Q

are all childrens feet flat at birth

A

yes

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12
Q

what does rigid flat foot usually imply

A

underlying bony abnormality

occasionally its a sign of serious disease such as RA

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13
Q

what is osgood schlatter’s disease

A

inflammation of the attachment of the patellar tendon to the growing tibial epiphysis

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14
Q

what causes the inflammation in osgood schlatter’s disease

A

excess traction by the quadriceps

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15
Q

what is rarely seen in adolescent knee pain

A

chondromalacia patellae - eroded area of patellar cartilage

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16
Q

eroded area of patellar cartilage

A

chondromalacia patellae

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17
Q

how common is CDH

A

one or two live births per thousand

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18
Q

is the hip usually completely dislocated at birth in CDH?

A

rarely

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19
Q

CDH more common in girls or boys?

A

girls

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20
Q

what kind of tendency is there in CDH

A

familial and racial

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21
Q

when should children be screened for CDH?

A

at birth
3 m
6m
12 m

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22
Q

clinical signs of CDH

A

limb shortening
asymmetrical creases
limited adduction
limp

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23
Q

what is the next step of action if the CDH test produces a click

A

re examination at 3 m in a specialist clinic - radiograph usually justified

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24
Q

next step of action if CDH is discovered late but before weight bearing

A

gentle traction followed by open or closed manipulation

followed by splintage for

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25
next step of action in CDH if discovered late and walking has commenced
major surgery to deepen the undeveloped acetabulum and re-angulate the femoral neck secondary arthritis is highly likely
26
when is the mild, postural form of club foot seen
after breech | usually easily corrected at birth by manipulation
27
what is the fixed form of club foot associated with
developmental abnormalities of nerves and muscles of the leg
28
initial tx for club foot
in both forms: gentle stretching in 2 phases 1. correction of hind foot equinus 2. corrects the mid and forefoot varus for 6 weeks
29
Until when do children with club foot need to be followed up
until their feet stop growing (around age 14)
30
why is follow up for club foot important?
late relapse requiring surgery is not uncommon
31
the affected foot in clubfoot is usually significantly larger than the normal foot - true or false?
false - usually SMALLER
32
is spina bifida occulta usually of significance?
usually not!
33
some people who are affected by spina bifida occult develop what? a very small number may get what?
some people get mechanical backache a very small number get tethering of the spinal cord to the higher lumbar vertebrae during growth ("diastamatomyelia")
34
what is diastamatomyelia?
tethering of the spinal cord to the higher lumbar vertebrae during growth
35
what is spina bifida cystica?
baby is born with the neural plate tissues open with little or no skin or bony cover
36
what do many children with spina bifida cystica also have?
hydrocephalus
37
hydrocephalus leads to mental retardation - t or f
true
38
whats it called when nerve tissue is covered by a cyst
meningocele | meningomyocele if nerve tissue is incorporated into cyst wall
39
can spina bifida cystica be life threatening?
yes, many children die at or soon after birth
40
long term complications of spina bifida cystica
paralysis growth deformities through muscle imbalance incontinence many are mentally retarded
41
many children with spina bifida cystic need early surgery to their ?
feet - to maintain a functional shape
42
if a child with spina bifida cystica develops joint contraction what can this result in?
fixed flexion of knees and dislocation of hips
43
children with spina bifida cystica should be encouraged to do minimal movement - t or f
false - they should keep mobile until adolescence so that they may grow to a reasonable size
44
in CP does spinal tissue develop normally?
yes, so they have uninhibited spinal reflexes
45
in terms of movement what do people with CP lack? what does this result in?
they lack co-ordination and purpose of movement normally controlled by the brain, resulting in a spastic type of paralysis
46
what causes joint deformity in CP
some muscles contract strongly (spastic) and some are weak and flaccid >> imbalance >> abnormal muscle and bone growth >> joint deformity
47
name of CP where 2 legs are affected
paraparesis
48
a common sign of minor degree of spasticity seen in adolescence
toe walking
49
splintage should be used frequently in CP - true or false?
false - it should be used with caution as too much can lead to increased muscle spasm and deformity
50
what is scoliosis
curvature of the spine with a rotary abnormality of the vertebrae
51
when do most cases of idiopathic scoliosis occur
adolescence
52
Is scoliosis more common in girls or boys?
far more common in girls
53
With scoliosis what does the child usually complain of?
twisting of the ribs which causes a hump on one side of the shoulder
54
do braces have a role in scoliosis
no
55
causes of a limp from birth
CDH | infection of the hip
56
cause of a limp between age 4 and 10
Perthe's
57
cause of a limp from 10 to 15
SUFE
58
what is Perthe's?
an osteochondritis of the femoral head epiphysis
59
what percentage of cases of Perthe's are bilateral
20%
60
presentation of Perthe's
painful limp followed by a slow recovery
61
what does U/S reveal in Perthe's
excess fluid in the hip joint
62
what is Perthe's thought to be caused by?
avascular necrosis of the growing femoral head
63
strategy of treatment in Perthe's
to maintain the head of the femur concentrically within the acetabulum until the disease runs its course
64
if involving up to half the femoral head, does Perthe's need tx?
no - prognosis is good
65
is prognosis for Perthe's better in younger or older children?
younger
66
what can be done in Perthe's to alleviate pain and limp?
traction
67
Who is SUFE seen in?
boys age 12 who are sexually immature for their age | girls a little older who have recently undergone an adolescent growth spurt
68
what nerve causes SUFE to sometimes cause knee pain?
obturator
69
is the limp always painful in SUFE?
no
70
what must radiographs in suspected SUFE include?
lateral view
71
management of SUFE
surgical - if minor slippage, pin in new deformed position - if major slippage, may attempt to replace the head although this comes with high risk of AVN - observe other hip!! pin if an sign of slippage
72
when are pins from SUFE surgery best to be removed?
after epiphyseal fusion at around 18 y/o