15.11.2 Skeletal Conditions Flashcards

1
Q

Rotational variations

A
  • Vary widely (varies until age of 5 -> mature gait)
  • Generally not pathological
  • Foot position during walking relative to the body’s line of movement during the gait cycle
  • Torsion➡️internal/ external / neutral
    ➡️version of the bones
    ➡️capsular pliability
    ➡️muscle control
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2
Q

Rotational variation Assessment

A

Static
- Available range of rotational motion
- Prone position

Dynamic
- Effect of various torsional
- Child should be able to walk alone Shoes and barefoot
- Foot and knee position should be observed over several cycles of gait.

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3
Q

Thigh foot angle

A
  • Degree of tibial torsion
  • Foot deformities may contribute to rotational abnormalities
  • The average TFA: (only understand there is a big variation in children)
    ➡️5 degrees internal in infants (range, -30 to +20 degrees)
    ➡️10 degrees external by 8 years of age (range, -5 to +30 degrees)
  • TFA changes very little after 12 years of age
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4
Q

Rotational profile

A
  • Foot progression angle
  • Static rotation
  • Thigh foot angle
  • Abnormal rotational profiles➡️2 standard deviations
  • According to Staheli’s criteria
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5
Q

Differential diagnosis

A

In-toeing
- Metatarsus adductus
- Internal tibial torsion
- Excessive femoral anteversion
- Children sit in W position (normal until 10 years; after this it won’t heal on its own)

Out-toeing
- femur or tibia turned outwards
- External rotation contracture of the hip (intra-uterine position) -18-24 month
- External femoral torsion Excessive ext tibial torsion
- Pes Planus
- Calcaneovalgus foot
- SCFE (sudden onset especially in older children) -> separation between femoral head and neck at growth plate

Genovarum (Don’t need to know all the names, only know what it is)
- Physiologic bowing
- Blounts disease
- Metabolic bone disease
➡️X linked Hypophosphatemic (XLH) rickets
➡️Nutritional rickets
Skeletal dysplasia
➡️Achondroplasia
➡️Pseudoachondroplasia
➡️Metaphyseal chondrodysplasia (Schmid’s or McKusick’s type)
- Neoplastic disease (rare)
- Trauma (sequelae)
- Infection(sequelae)

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6
Q

Alignment variations

A
  • Natural history is gradual normalization➡️by 6 to 7 years of age
  • 99% resolve spontaneously
  • Tibia torsion surgically addressed after age 8
  • Femoral anteversion addressed after age 10

Straight at 8 - Alignment should be straight at age of eight (Slide 11)

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7
Q

Physiological bowing

A
  • At birth: 10 to 15 degrees of varus
  • 10 degrees of bilateral femoral-tibial varus noted after the age of 18 months.
  • Associated internal tibial torsion
  • Early walkers

Clinical features
- A family history is common
- Bilateral, it may be asymmetric
- Very agile walkers
- NO Dynamic varus/ lateral thrust should be noted➡️characteristic of pathological bowing

Role of X-rays
- NOT before 18 months of age
- > 18 months- essential part of the evaluation
- Specifically Indicated:
➡️pronounced deformities (clinical femoral-tibial angle >20°) ➡️lateral thrust is observed
➡️short stature (below fifth percentile)
➡️metabolic bone disease is suspected
- Distribution of bowing deformity is noted
- Physiologicbowing throughout the distal femur, proximal tibia and distal tibia.
- Early Blount diseaseproximal tibia

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8
Q

Genu Valgum

A
  • can be physiological
  • 3-4 years of age children have up to 20 degrees of genu valgum
  • Genu valgum rarely worsens after age 7
  • After age 7 valgus should not be worse than 12 degrees

Unilateral genu valgum
- Physeal injury from trauma, infection, or vascular insult
- Tibia fractures
- Benign tumors

Bilateral genu valgum
- Physiologic
- Renal rickets
- Skeletal dysplasia

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9
Q

Packaging disorders
Torticollis
Genu recurvatum

A

If you see one, you should check for the other one

Torticollis
- Present at birth
- Head is tilted towards the affected side but the chin away from the affected side
- Shortened Sternocleidomastoid muscle
- Breastfeed/ feed and carry the child to encourage stretching of the affected side
- Physiotherapy referral for stretching.
- If not resolved by the age of 1, will need surgery.

Genu recurvatum
- Present at birth
- Spectrum of disease
- Breech babies
- Associated with syndromes
- Resolves with time
- Management is splinting
- Refer at 6 weeks of age to assess and ultrasound the hips for DDH
- If flexion <30 degrees achieved, need soft tissue releases

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10
Q

Tibial bowing

A
  • All need to be referred to the Orthopaedics.
  • Anterolateral bowing is most likely to be caused by
    Neurofibromatosis.
  • AnteroMedial bowing is most likely due to hemiMelia.
  • Posterolateral bowing resolves with time but needs to be followed up.
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11
Q

Common hip pathology
DDH - developmental dysplasia of the hip

A

DDH
- First born
- Female
- breech
- family history
- positive ortolani and barlow
- refer for ultrasound at 6 weeks (no X-ray because bone is not calcified yet, see better on ultrasound)

Late presenter
- Leg length discrepancy
- Waddling gait if bilateral
- These need x rays and referral for surgery!

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12
Q

Perthes

A
  • 4-8 years
  • Boys
  • AVN (idiopathic) of femoral head which remodels
  • Must exclude TB (and other causes of AVN)
  • Please always do CRP and ESR

RF for poor prognosis
- Female
- Older than 8 years on presentation
- Stiff hip

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13
Q

SUFE

A

Teen with knee pain who is not sporty

  • Knee pain in adolescents
  • Usually 12-14 years but as early as 8!
  • Overweight usually
  • Strict non-weight bearing
  • Semi-urgent referral to Ortho
  • VULA!
  • patient is told not to walk and need to be referred so that head can be pinned
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