Limp & Gait Disorders – Clinical Scenario with Lab & Imaging
A 6-month-old infant with asymmetric thigh folds and limited hip abduction on the left. No fever, no pain.
Q1
Identify the most likely diagnosis based on the clinical presentation and lab findings.
WBC
6.5 × 10³/µL (normal)
ESR
10 mm/hr (normal)
CRP
0.1 mg/dL (normal)
✅ Model Answer:
• Diagnosis: Developmental Dysplasia of the Hip (DDH) — asymmetric thigh folds, limited hip abduction on the left, normal inflammatory markers. No fever, no pain. Hip ultrasound (Graf) shows alpha angle <60° (dysplastic), beta angle >55° (subluxated/dislocated).
• Any other test: Hip ultrasound (Graf method) — alpha angle (normal >60°), beta angle (normal <55°). Pelvic X-ray (after 4-6 months for ossific nucleus — but ultrasound is preferred in infants <6 months).
• What to do next: Start Pavlik harness (for infants <6 months) — maintain hips in 90-100° flexion and neutral abduction. Full-time wear for 6 weeks, then wean. Follow-up ultrasound weekly.
• Follow-up plan: Monitor with ultrasound every 1-2 weeks to confirm concentric reduction. If no reduction after 3-4 weeks → consider closed reduction and spica cast. Long-term: monitor for residual acetabular dysplasia.
Q2
What is Developmental Dysplasia of the Hip (DDH)?
✅ Model Answer:
• DDH is a spectrum of hip disorders ranging from mild acetabular dysplasia to complete hip dislocation.
• Pathophysiology: The femoral head is not properly seated in the acetabulum → abnormal development of the hip joint.
• Spectrum:
- Dysplasia: Shallow acetabulum (femoral head is still in the joint but not well covered).
- Subluxation: Partial displacement of the femoral head from the acetabulum.
- Dislocation: Complete loss of contact between the femoral head and acetabulum.
• Incidence: 1-2 per 1000 live births (more common in females, breech presentation, positive family history).
• Risk factors:
- Breech presentation (especially frank breech)
- Female sex (4-5:1)
- Family history of DDH
- Firstborn (due to uterine constraint)
- Oligohydramnios
- Congenital torticollis, metatarsus adductus (associated conditions)
Q3
What are the clinical features of DDH in infants?
✅ Model Answer:
• Clinical features:
- Asymmetric thigh folds: Unequal number or depth of skin folds on the medial thighs.
- Limited hip abduction: The affected hip cannot be abducted to 70-80°.
- Galeazzi sign: The affected knee is lower than the contralateral when the hips are flexed (femoral shortening).
- Ortolani maneuver: A palpable "clunk" when the hip is reduced (abduction and forward pressure on the femoral head).
- Barlow maneuver: A palpable "clunk" when the hip is dislocated (adduction and backward pressure).
- Limb length discrepancy: Shortening of the affected limb.
- Limited range of motion: Hip stiffness.
- No fever, no pain.
- Waddling gait: In older children (after walking age).
- Trendelenburg sign: Pelvic drop when standing on the affected leg.
Q4
What is the role of hip ultrasound in diagnosing DDH?
✅ Model Answer:
• Hip ultrasound (Graf method): The imaging modality of choice for infants <6 months (before the femoral head ossifies).
• Measurements:
- Alpha angle: Angle of the acetabular bony roof (normal >60°).
• >60° = normal
• 50-60° = mild dysplasia (type II)
• <50° = severe dysplasia (type III/IV)
- Beta angle: Angle of the acetabular cartilage (normal <55°).
• <55° = normal
• >55° = subluxation/dislocation
• Types:
- Type I: Normal (alpha >60°, beta <55°).
- Type II: Dysplastic (alpha 50-60°, beta <55°).
- Type III: Subluxated (alpha <50°, beta >55°).
- Type IV: Dislocated (alpha <50°, beta >55°).
• Advantages: No radiation, dynamic assessment of the hip.
• Disadvantages: Operator-dependent, requires experienced sonographer.
Q5
What is the management of DDH in infants?
✅ Model Answer:
• Pavlik harness (for infants <6 months): The standard treatment for reducible DDH.
- Position: Hips in 90-100° flexion and neutral abduction (not forced abduction).
- Wear: Full-time (24 hours/day) for 6 weeks, then wean to part-time (12-16 hours/day) for another 6 weeks.
- Monitoring: Ultrasound every 1-2 weeks to ensure concentric reduction.
- Success rate: 85-95% if started early (<6 months).
• Failed harness: If reduction is not achieved after 3-4 weeks.
• Closed reduction + spica cast: For infants 6-18 months.
- Procedure: Reduction under general anesthesia → spica cast for 3-4 months.
- Timing: Usually done at 6-18 months.
• Open reduction + pelvic osteotomy: For children >18 months or failed closed reduction.
• Contralateral hip: Should be screened (bilateral in 20-40%).
Q6
What is the role of X-ray in DDH?
✅ Model Answer:
• X-ray (AP pelvis): Used after 4-6 months of age (when the femoral head ossifies).
• Findings:
- Normal: Femoral head is centered in the acetabulum, Shenton's line is intact.
- DDH:
• Shenton's line: Disrupted (the femoral neck and superior pubic ramus do not form a continuous arc).
• Acetabular index: Increased (>30° in infants, >25° in older children).
• Femoral head: Displaced laterally and superiorly (subluxation/dislocation).
• Delayed ossification: Smaller ossific nucleus on the affected side.
• Centre-edge angle of Wiberg: <20° (in children >5 years) indicates dysplasia.
• Limitations: X-ray is less sensitive than ultrasound in infants <6 months; ultrasound is the preferred modality.
Q7
What are the complications of untreated DDH?
✅ Model Answer:
• Complications:
- Premature osteoarthritis: Most common long-term complication — due to abnormal joint mechanics.
- Leg length discrepancy: Shortening of the affected limb.
- Limp (Trendelenburg gait): Due to abductor weakness and hip instability.
- Pain: Hip pain in adolescence and adulthood.
- Decreased range of motion: Hip stiffness.
- Avascular necrosis (AVN): Of the femoral head (if treatment is delayed or reduction is forceful).
- Acetabular dysplasia: Residual shallow acetabulum (may require pelvic osteotomy later).
- Pathologic fracture: Weakening of the bone.
- Permanent disability: If untreated, can lead to severe functional impairment.
- Total hip replacement: May be needed in adulthood if severe osteoarthritis develops.
Q8
What is the prognosis and long-term outcome for children with DDH?
✅ Model Answer:
• Prognosis:
- Excellent: If diagnosed and treated early (<6 months) with Pavlik harness (85-95% success).
- Good: If treated between 6-18 months with closed reduction and spica cast.
- Guarded: If treated after 18 months or if there is residual dysplasia.
- Residual dysplasia: May require pelvic osteotomy later in childhood.
- Risk of osteoarthritis: Higher if residual dysplasia persists.
- Life expectancy: Normal.
• Long-term follow-up:
- Orthopedic: Follow-up X-rays every 6-12 months until skeletal maturity.
- Monitor for residual dysplasia: Acetabular index, centre-edge angle.
- Monitor for AVN: If treatment was delayed or forceful.
- Physical therapy: To maintain hip range of motion and strength.
- Activity modification: Avoid high-impact sports if residual dysplasia is present.
- Long-term: Risk of premature osteoarthritis — may require hip replacement in adulthood (40-60 years).
⚠️ Key Concept: Developmental Dysplasia of the Hip
• Asymmetric thigh folds + limited abduction + normal labs = DDH.
• Diagnosis: Hip ultrasound (alpha angle <60°, beta angle >55°).
• Management: Pavlik harness (for infants <6 months) — 85-95% success.
• Complications: Premature osteoarthritis, leg length discrepancy, AVN.
• Prognosis: Excellent with early treatment; monitor for residual dysplasia.
🎯 Examiner Scoring Checklist
• Identifies DDH (asymmetric thigh folds, limited abduction, normal labs)
• Orders hip ultrasound (Graf — alpha/beta angles)