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Unilateral shortening/tightness of the SCM causing an asymmetrical head position
Congenita Muscular Torticollis (CMT)
SCM shortening
1. Lateral flexion on the same side
2. Rotate to the opposite direction
In a 6-month-old child demonstrating muscle contracture consistent with Left torticollis, what is the BEST stretching technique to normalize muscle length of thesternocleidomastoid?
Stabilize the left shoulder and stretch the neck into right side-bending and Left rotation
Classification for cranial deformation
Deformational plagiocephaly
Deformational Brachycephaly
Deformational Dolichocephaly
What is deformational plagiocephaly (DP)?
Ipsilateral occipital flattening
What is deformational brachycephaly (DB)?
Central occipital flattening associated with prolonged supine positioning
What is deformational dolichocephaly (DD)?
A disproportionately long and narrow skull, commonly associated with prematurity
Classification for CMT: 3 types
Postural CMT
Muscular CMT
Most severe form involving an SCM nodule/fibrous band
What characterizes postural CMT?
Mildest form; positional preference without PROM limitation or an SCM nodule
What characterizes muscular CMT?
Unilateral SCM tightness during lateral flexion and/or rotation without an SCM nodule
What characterizes the most severe CMT classification?
Palpable SCM nodule/fibrous bands with limited cervical rotation and/or lateral flexion
Grade 1 CMT Early Mild
0-6 months + only postural preference OR <15° difference in passive cervical rotation
Grade 2 CMT Early moderate
0-6 months + 15-30° difference in passive cervical rotation
Grade 3 CMT Early severe
0-6 months + >30° rotation difference OR an SCM mass
Grade 4 CMT Later mild
7-9 months + postural preference OR <15° rotation difference
Grade 5 CMT Later moderate
10-12 months + postural preference OR <15° rotation difference
Grade 6 CMT Later severe
7-9 months + >15° difference OR 10-12 months + 15-30° difference
Grade 7 CMT Later extreme
7-12 months + SCM mass OR 10-12 months + >30° rotation difference
Grade 8 CMT Very late
>12 months with any asymmetry: postural preference, ROM difference, or SCM mass
What UE functional limitations may occur on the involved side?
Difficulty with UE weight bearing and reaching toward midline
What other musculoskeletal asymmetries can occur with CMT?
Trunk curvature toward the affected SCM and persistence of the asymmetric tonic neck reflex
Cervical strength: Muscle function test Scale
0 = with the head below horizontal,
1 = with the head on the horizontal line,
2 = with the head slightly over the horizontal line,
3 = with the head high over the horizontal line
4 = with the head very high over the line approaching vertical
What are the major PT interventions for CMT?
Positioning, stretching, parent education, active/passive ROM, strengthening, and symmetrical movement activities
Recommended Interventions for Cranial Deformation: Brachycephaly
Inc prone positioning to relieve pressure on occiput to allow for reshaping
Recommended Interventions for Cranial Deformation: Plagiocephaly
Head turning and positioning opposite of preferred position, inc time in prone, facilitation of development to encourage overall movement away from flattened side
What is the first-choice intervention for CMT with strong evidence?
Caregiver education, environmental adaptations, PROM, neck/trunk AROM, and symmetrical movement activities
What are the main conservative interventions for cranial deformation under 6 months?
Parent/caregiver instruction in and adherence with repositioning, inc supervised prone play while awake, environmental adaptations, Cranial remolding therapy is indicated for infants with moderate to severe CD at 3-6 months of age or older
How long are cranial orthoses typically worn per day?
20-23.5 hours/day
How long may cranial remolding therapy last?
2-7 months for optimal outcomes
What is the CMT stretch for a left tight SCM?
R tilt and L rotation
What is the CMT stretch for a right tight SCM?
L lateral flexion with R rotation
What is the general stretching frequency for 1-person passive stretching?
2-3 times/day, 5-15 repetitions, with 1-10-second holds
What is the general frequency for 2-person passive stretching?
4-8 times/day, with at least 30-40 repetitions per set
If CMT is not resolving after 4-6 weeks of therapy
referral back to the physician be considered
What are indications for surgical management of CMT?
No improvement after 6 months
Residual head tilt
≥15° PROM deficit
Tight muscular band
When is surgery most likely to have a positive outcome?
Between 10 months and 5 years of age
Face Legs, Activity, Cry, and Consolability scale (FLACC)
Used to assess pain in infants, young children
What is the FLACC score range?
0-10
FLACC — Face = 0
No particular expression or smile.
FLACC — Face = 1
Occasional grimace or frown, withdrawn, disinterested
FLACC — Face = 2
Frequent to consistent quivering chin, clenched jaw
FLACC — Legs = 0
Normal position or relaxed
FLACC — Legs = 1
Uneasy, restless, tense
FLACC — Legs = 2
Kicking or legs drawn up
FLACC — Activity = 0
Lying quietly, normal position, moves easily
FLACC — Activity = 1
Squirming, shifting back and forth, tense
FLACC — Activity = 2
Arched, rigid, or jerking
FLACC — Cry = 0
No cry (awake or asleep)
FLACC — Cry = 1
Moans or whimpers; occasional complaint
FLACC — Cry = 2
Crying steadily, screams, or sobs; frequent complaints
FLACC — Consolability = 0
Content, relaxed
FLACC — Consolability = 1
Reassured by occasional touching, hugging, or being talked to
FLACC — Consolability = 2
Difficult to console or comfort
An autoimmune inflammatory disorder in which the body mistakenly identifies some of its own cells/tissues as foreign. It is the most common rheumatic disease of childhood
Juvenile Idiopathic Arthritis (JIA)
What are the diagnostic characteristics of JIA?
Begins before age 16
Persists for >6 weeks
Cause is unclear
No definitive laboratory test
Diagnosis is primarily based on clinical signs/symptoms during the first 6 months
What are the 3 most common types of JIA?
1. Oligoarticular (pauciarticular)
2. Polyarticular
3. Systemic
What are common signs/symptoms of JIA?
Inflammation causing redness, heat, pain, and swelling
What long-term problems can JIA cause?
Chronic joint swelling
Pain
Limited ROM
Muscle atrophy/weakness
Poor aerobic function
Impaired exercise tolerance
Postural abnormalities
Gait deviations
Activity/participation restrictions
Reduced QOL
What is the most common type of JIA?
Oligoarticular (pauciarticular) JIA
How many joints are affected in oligoarticular JIA?
Four or fewer joints, with low-grade inflammation
Who is commonly affected by oligoarticular JIA?
Girls 2-4 years
Which joints are most commonly affected in oligoarticular JIA?
Knee, ankle, elbow
What is an important eye complication of oligoarticular JIA?
Iridocyclitis, an inflammation of the iris and ciliary body
Arthritis involving 5 or more joints
Polyarticular JIA
How is polyarticular JIA subdivided?
Into rheumatoid factor (RF)-positive and RF-negative polyarthritis
What functional problem can severe polyarticular JIA cause in the hands?
Difficulty fully extending the fingers due to joint involvement/contractures
What is the hallmark diagnostic feature of systemic JIA?
Spiking fever ≥39°C (102.2°F) occurring once or twice daily, typically in the afternoon/evening, for at least 2 weeks accompanied by a rash
What are the major goals of PT intervention for JIA?
Maintain/preserve joint function
Restore or compensate for function/activity
Manage pain
Prevent deformity
Maintain/improve ROM
Strengthen
Improve proprioception
Protect joints
Promote functional abilities
Improve physical fitness
What is the treatment for a 0-2 cm leg length inequality?
No treatment
What is the treatment for a 2-4 cm leg length inequality?
Shoe lift
What is the treatment for a 2-6 cm leg length inequality?
Epiphysiodesis or shortening
What is the treatment for a 6-20 cm leg length inequality?
Lengthening, possibly combined with other procedures
What is the treatment for a leg length inequality >20 cm?
Prosthetic fitting
Therapy intervention for the acute phase
Child and family education
Pain management, deformity prevention
ROM maintenance or improvement, strengthening, proprioceptive training
Joint protection strategies
Promotion of functional abilities
Physical fitness
What intervention is used for morning stiffness in JIA?
Movements of any kind, especially movement in the extension direction of joints and stretching of biarticular muscles
What intervention is used to improve joint ROM in JIA?
Gentle movements of any kind, especially movements in the extension direction of joints and stretching of biarticular muscles
What intervention is used for decreased muscle strength in JIA?
Isometric and isokinetic muscle-strengthening exercises
What intervention is used to improve health-related physical fitness in JIA?
Aerobic
What interventions can be used for pain behaviors in JIA?
Relaxation with mindfulness, tai chi, or qigong
What intervention can be used to address gait problems in JIA?
Insoles (soft or supinating, retrocapital support) or rocker-bottom external soles
T or F: Full extension is only restored when the intraarticular effusion ( joint swelling) has disappeared
T
An adolescent with polyarticular JIA is clinically stable with minimal morning stiffness. Which aerobic prescription is MOST appropriate?
A. 10 minutes of jump training at 85-90% HRmax, 6-7 days/week
B. 20-30 minutes of cycling or swimming at moderate intensity, 3-5 days/week
C. Isometric only; avoid all aerobic activity
D. Treadmill running to pain tolerance, 5 days/week
B. 20-30 minutes of cycling or swimming at moderate intensity, 3-5 days/week
A 10-year-old with known JIA develops daily spiking fevers, a salmon-colored rash, and reports chest pain with shortness of breath during your session. What is the BEST action?
A. Continue with low-intensity cycling and monitor symptoms
B. Stop therapy and arrange urgent medical evaluation
C. Apply moist heat and begin diaphragmatic breathing
D. Instruct home rest and recheck next visit
B. Stop therapy and arrange urgent medical evaluation
A 7-year-old with known juvenile idiopathic arthritis has a medically confirmed flare affecting the right knee. The knee is warm and swollen, with pain at end-range motion. Which PT intervention is MOST appropriate during this session?
A. High-load isotonic quadriceps training and aggressive stretch
B. Prolonged immobilization in a knee immobilizer during the day
C. Pain-free AROM, cold application post-session, and a night extension splint
D. Continuous ultrasound (1.5 W/cm²) over the distal femoral physis
C. Pain-free AROM, cold application post-session, and a night extension splint
A child is newly diagnosed with juvenile idiopathic arthritis and reports no eye symptoms. Which screening referral should be arranged early?
A. Echocardiogram for cardiomyopathy
B. Slit-lamp eye exam by ophthalmology
C. DEXA scan for low bone density
D. EMG for peripheral neuropathy
B. Slit-lamp eye exam by ophthalmology
A 4-year-old girl has a painless swollen left knee and intermittent ankle swelling for 3 months. Which JIA subtype is MOST likely?
A. Systemic JIA
B. Enthesitis-related JIA
C. Oligoarticular (pauciarticular) JIA
D. Polyarticular JIA
C. Oligoarticular (pauciarticular) JIA
A congenital, nonprogressive neuromuscular disorder characterized by joint contractures in 2 or more body areas, often associated with muscle weakness
Arthrogryposis Multiplex Congenita (AMC)
Clinical signs of AMC
Severe joint contractures and lack of muscle development
Limit participation in even basic ADLs
What are common musculoskeletal findings in AMC?
Hip flexion/dislocation
Knee contractures
Clubfeet/equinovarus
Internally rotated shoulders
Flexed elbows
Flexed/ulnar-deviated wrists
Muscle hypoplasia/weakness
What are the major components of early PT management for AMC?
Vigorous stretching
Splinting
Positioning
Strengthening
Developing optimal positions for ADLs and motor skill development
Which finding is MOST consistent with AMC?
A. Hyperreflexia and velocity-dependent tone
B. Multiple rigid joint contractures with muscle hypoplasia and normal cognition
C. Fluctuating weakness with fatigability worsened by activity
D. Recurrent joint effusions and warmth
B. Multiple rigid joint contractures with muscle hypoplasia and normal cognition
A group of genetic disorders causing fragile bones, usually due to problems with type I collagen
Osteogenesis Imperfecta (OI)
What is a classic ocular finding in OI?
Blue-gray or blue sclerae
What other features may occur with OI?
Short stature, bone deformity, joint laxity, and hearing loss
OI Type I
Mildest form
Few to multiple fractures, little bone deformity, blue/gray sclerae, and near-normal height/life expectancy
When do Type I fractures often decrease?
After puberty
OI Type II
Most severe
Extremely fragile bones, bowed/crumpled long bones, poor chest development, and pulmonary insufficiency
Why do many infants with OI Type II die early?
Respiratory failure related to underdeveloped lungs
OI Type III
Severe progressive deformity, frequent fractures, short stature, and substantial mobility limitations
What may contribute to breathing problems in OI Type III?
Spinal and chest wall deformities