Childrens Orthopaedics Flashcards

1
Q

give 4 congenital foot conditions?

A

clubfoot
rocker bottom foot
neurofibromatosis
skeletal dysplasia

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2
Q

give 4 neuromuscular disorders of feet

A

cerebral palsy
tip toe walking
Duchenne muscular dystrophy
high arch (cavus)

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3
Q

what are the 4 features of clubfoot?

A
CAVUS
Cavus
Adductus
Varus
Equinus
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4
Q

what is clubfoot and what causes it?

A

birth defect causing abnormal foot posture

can be idiopathic or associated with other more serious conditions

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5
Q

what is postural talipes?

A

normal curved posture of newborns

looks like clubfoot but can be forced into normal position

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6
Q

how is clubfoot treated?

A

ponseti method of casting

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7
Q

what is rocker bottom feet?

A

congenital vertical talus due to irreducible dislocation of talus on navicular

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8
Q

what are the features of rocker bottom feet?

A

round plantar features

equinus hindfoot

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9
Q

common feature of clubfoot and rocker bottom feet?

A

fixed ankle equinus

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10
Q

what is neurofibromatosis?

A

congenital disorder affecting extremities, spine and skin

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11
Q

what causes neurofibromatosis?

A

autosomal dominant inheritance of NFI gene Ch17

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12
Q

how is neurofibromatosis diagnosed?

A
2 out of the following 7 present
>6 café au lait spots
2 or more neurofibromas/plexiform neurofibromas
freckling axilla/inguinal region
optic glioma
2 or more lisch nodules
cortical thinning/pseudoarthrosis
first degree relative affected
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13
Q

what is skeletal dysplasia?

A

congenital disorders involving bone and cartilage

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14
Q

what are the features of skeletal dysplasia?

A
shortening of involved bone
short stature (usually <2 SD)
- can be proportionate or disproportionate
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15
Q

what is the most common form of skeletal dysplasia?

A
achondroplasia
normal trunk/short limbs
frontal bossing
genu varum
normal intelligence
motor delay
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16
Q

what causes achondroplasia?

A

fibroblast growth factor receptor 3 FGFR3

either autosomal dominant or spontaneous mutation

17
Q

what is cerebral palsy?

A

non-progressive neuromuscular disorder causing injury to immature brain (<2 years)

  • prematurity
  • perinatal (infection, injury, meningitis)
18
Q

what are the features of cerebral palsy?

A
UMN disease (muscle weakness/spasticity)
early = abnormal muscle forces > dynamic deformity
late = contractures, deformity, dislocation
head unaffected?
19
Q

what is clasp knife spasticity?

A

where abnormally increased resistance to stretching of a muscle gives way abruptly, usually near the end of the range of joint movement
seen in cerebral palsy

20
Q

how is cerebral palsy functionally diagnosed?

A

walking

non-walking

21
Q

how can cerebral palsy be treated?

A

benzodiazepines baclofen
selective dorsal rhizotomy
botulinum toxin

22
Q

what is Duchenne muscular dystrophe?

A

commonest muscular dystrophy

X linked recessive disorder causing progressive muscle weakness

23
Q

what causes duchenne muscular dystrophe?

A

absence of dystrophin protein

replacement of muscle with fibrofatty tissue

24
Q

how does Duchenne muscular dystrophy present?

A
2-5 yrs old
muscle weakness (prox > distal)
clumsy walking
positive gowers sign
scoliosis
25
Q

how is Duchenne muscular dystrophe diagnosed?

A
creatinine phosphokinase
muscle biopsy (absence of dystrophin)
26
Q

what is gowers sign?

A

cant stand up from knees alone

use hands to walk up the legs to stand upright

27
Q

what is cavus feet?

A
pes cavus (high arched foot)
elevated longitudinal arch and varus hindfoot
28
Q

what causes cavus feet?

A

idiopathic/familial
2/3 due to neurological disorder (polio, cerebral palsy, myelomeningocoele, SCI)
charcot marie tooth

29
Q

how is cavus feet assessed?

A

X rays

Coleman block test

30
Q

how is cavus feet managed?

A

conservative
surgery
- soft tissue
- bony (osteotomy)