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519750
Abnormal posture
Description
Paediatrics (MSK) Mind Map on Abnormal posture, created by v.djabatey on 01/02/2014.
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msk
paediatrics
paediatrics
msk
Mind Map by
v.djabatey
, updated more than 1 year ago
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Created by
v.djabatey
almost 11 years ago
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Resource summary
Abnormal posture
talipes equinovarus (clubfoot)
positional talipes
from intrauterine compression
common
normal-sized foot
mild deformity
corrected to neutral position w/ passive manipulation
if marked, physio can show parents passive exercises
abnormalities
entire foot inverted & supinated
forefoot adducted
heel internally rotated and in plantar flexion
affected foot shorter than normal
calf mm thinner than normal
position of foot is fixed
can't be completely corrected
often bilateral
epidemiology
birth prevalence 1 per 1000 live births
mostly males affected M:F= 2:1
causes
idiopathic
familial
2ndary to oligohydramnios during pregnancy
malformation syn or neuromuscular disorder
spina bifida
spinal lesion
assoc w/ developmental dysplasia of hip (DDH)
Rx
Ponsetti method
plaster casting & bracing
may be needed for many months
usually successful
if severe, corrective surgery
vertical talus
stiff foot
rocker-bottom shape
need to differentiate this from talipes equinovarus
other malformations common
X-ray
confirm diag
usually needs surgery
flat feet
rigid flat foot pathological in older kids & teens
suggested by absence of normal arch on tip toeing
causes
tendo-Achilles contracture (ankle)
tarsal coalition
inflammatory arthropathy (JIA)
tarsal coalition
due to lack of segmentation btw 1 or more bones of foot
coalitions that were fibrous or cartilaginous get symptomatic as they start to ossify
progressively get more rigid & limit normal foot motion
get symptomatic during pre-teen years
normal radiographs if bars haven't yet ossified
corrective surgery
pes cavus
high arched foot
presentation in older kids assoc w/ neuromuscular disorders
Friedrich ataxia
type I hereditary motor sensory neuropathy (peroneal muscular atrophy)
Rx needed if foot stiff or painful
developmental dysplasia of hip (DDH)
spectrum of disorders
ranging from dysplasia to frank dislocation of hip
early detection important
cos DDH responds to conservative Rx
neonatal screening as part of routine examination of newborn
Barlow manoeuvre
checks if hip can be dislocated posteriorly out of acetabulum
repeat @ 8 weeks old
Ortolani manoeuvre
checks if hip can be relocated back into acetabulum
repeat @ 8 weeks old
hip abnormality detected on neontal screening
6-10 per 1000 live births
some cases missed
examiner inexperience
sometimes not possible to detect dislocation @ this stage e.g. if only mildly shallow acetabulum
can use ultrasound screening to overcome this
highly specific in detecting DDH
expensive
high false + rate
not recommended in UK
late diagnosis usually assoc w/ hip dysplasia
needs complex Rx incl surgery
presentation after neonatal period
usually as limp or abnormal gait
IDed from
asymmetry of skinfolds around hip
limited abduction of hip
shortening of affected leg
true birth prevalence= 1.3 1000 live births
diag
if ?DDH refer to orthopaed specialist
ultrasound
detailed assessment of hip
quantify degree of dysplasia
subluxation or dislocation present?
if initial US abnormal
place infant in splint or harness
keep hip flexed & abducted for several months
expert to do splinting
potential complication of splinting
necrosis of femoral head
Mx
splinting
harness
US or X-ray
monitor progress
surgery
if conservative measures
torticollis (wry neck)
sternocleidomastoid tumour (congenital muscular torticollis)
commonest cause in infants
occur in 1st few weeks of life
presentation
mobile, non-tender nodule
palpable within body of SCM
restriction of head turning
tilting of head
usually resolves in 2-6 months
passive stretching advised
but unproven efficacy
cause of presentation in childhood (i.e. after infancy)
muscular spasm
secondary to
ENT infection
spinal tumour
osteoid osteoma
cervical spine malformation or malformation
posterior fossa tumour
scoliiosis
= lateral curvature in the frontal plane of spine
structural scoliosis
rotation of vertebral bodies
causes prominence in back from rib asymmetry
changes often mild, pain-free and mainly cosmetic prob
severe cases
spinal curvature ->chest distortion
-> cardiorespiratory failure
causes
idiopathic
commonest cause
early onset (< 5 years old)
late onset
most often
mainly girls 10-14 years old
during pubertal growth spurt
congenital
from congenital structural defect of spine
hemivertebra
spina bifida
syndromes
e.g. VACTERL assocn- vertebral, anorectal, cardiac, tracheo-oesophageal, renal & limb anomalies)
secondary to
disorders of neuromuscular imbalance
cerebral palsy
muscular dystrophy
disorders of bone
neurofibromatosis
connective tissue disorders
Marfan's syn
leg length discrepancy
e.g arthritis of 1 knee in JIA
examination
start w/ inspection of child's back while standing up straight
irregular skin creases
differences in shoulder height
examine child's back when bent forward
to ID scoliosis
rib rotation seen (caused by vertebral rotation)
if scoliosis disappears
= postural scoliosis
but check leg lengths too
Mx
mild scoliosis will resolve spontaneously or progresses minimally
mod-severe
X-ray
to assess severity & progression of spine curvature
severe cases
specialist spinal centres
bracing
surgery
if severe
if coexisting pathology e.g.
neuromuscular disease
respiratory disease
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